12-bromododecanal

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromododecanol (5 g) dissolved in methylene chloride (30 ml) were added Celite (5.0 g) and pyridinium chlorochromate (5.2 g), and the mixture was stirred at room temperature for 12 hours. Then, .the reaction mixture was filtered and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give 12-bromododecanal (4.4 g). To 12-bromododecanal (4.4 g) dissolved in methylene chloride (50 ml) was added (carbomethoxymethylene)triphenylphosphorane (6.75 g), and the mixture was stirred for 4 hours. Then, the reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.91 g). The product was dissolved in acetonitrile (30 ml), and 1M tetra-n-butylammonium chloride in THF (27 ml) and potassium fluoride (7.6 g) were added. The mixture was heated under reflux for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexaneethylacetate 100:1 to give the methyl ester of 14-fluoro-3-tetradecenoic acid (3.3 g). Then, the reaction mixture was concentrated the residue thus obtained

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromododecanol (5 g) dissolved in methylene chloride (30 ml) were added Celite (5.0 g) and pyridinium chlorochromate (5.2 g), and the mixture was stirred at room temperature for 12 hours. Then, .the reaction mixture was filtered and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give 12-bromododecanal (4.4 g). To 12-bromododecanal (4.4 g) dissolved in methylene chloride (50 ml) was added (carbomethoxymethylene)triphenylphosphorane (6.75 g), and the mixture was stirred for 4 hours. Then, the reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.91 g). The product was dissolved in acetonitrile (30 ml), and 1M tetra-n-butylammonium chloride in THF (27 ml) and potassium fluoride (7.6 g) were added. The mixture was heated under reflux for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexaneethylacetate 100:1 to give the methyl ester of 14-fluoro-3-tetradecenoic acid (3.3 g). Then, .the reaction mixture was filtered

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromo-1-dodecanol (5 g) dissolved in methylene chloride (70 ml) were added pyridinium chlorochromate (10.1 g) and Celite (11.0 g), and the mixture was stirred at room temperature for 12 hours. Then, the reaction mixture was filtered, concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (20:1) to give 12-bromo-1-dodecanal (3.72 g). To the product dissolved in methylene chloride (50 ml) was added (carbomethoxymethylene)triphenylphosphorane (8.80 g), and the mixture was stirred. The reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (20:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.14 g). The product was dissolved in methanol and stirred under hydrogen atmosphere in the presence of palladium/carbon (1.5 g) for 18 hours. The reaction mixture was filtered and concentrated to give the methyl ester of 14-bromotetradecanoic acid (3.25 g). To the methyl ester dissolved in acetonitrile were added calcium chloride (12.3 g) and tetraethylammonium chloride (3.7 g), and the mixture was stirred at 80° C. for 3 hours, and then cooled and concentrated. The residue was distributed into ethyl acetate and water, and the ethyl acetate layer was dried and concentrated to give the methyl ester of 14-chlorotetradecanoic acid (2.37 g). 50% Aqueous ethanol (100 ml), in which potassium hydroxide (2.90 g) had been dissolved, was added to the methyl ester, and the mixture was stirred at 60° C. for 1 hour. Ethanol in the reaction mixture was evaporated, and the residue was acidified to a weak acidic range of pH by adding citric acid and extracted with ethyl acetate. The organic layer was dried and concentrated to give 14-chlorotetradecanoic acid (2.02 g). After the product was dissolved in N,N-dimethylformamide (DMF, 50 ml), para-nitrophenol (1.07 g) and N,N'-dicyclohexylcarbodiimide (1.59 g) were added, and the mixture was stirred for 12 hours. Then, precipitates produced was removed by filtration and the DMF was removed by distillation. The residue was subjected to chromatography on a silica gel column with eluent systems of n-hexane-ethyl acetate (from 200:1 to 50:1 ) to give the active ester of 14-chlorotetradecanoic acid (1.86 g). The active ester (500 mg) was dissolved in DMF (30 ml), and 6-(4'-N-glycyl-spicaminyl-amino)purine hydrochloride (500 mg) and triethylamine (2.0 ml) were added to the solution. The mixture was stirred for 12 hours. After the solvent was evaporated, the residue was subjected to chromatography on a silica gel column with eluent systems of chloroform-methanol (from 7:1 to 5:1) to give SPK280 in the yield of 247 mg. Then, the reaction mixture was filtered concentrated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromododecanol (5 g) dissolved in methylene chloride (30 ml) were added Celite (5.0 g) and pyridinium chlorochromate (5.2 g), and the mixture was stirred at room temperature for 12 hours. Then, .the reaction mixture was filtered and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give 12-bromododecanal (4.4 g). To 12-bromododecanal (4.4 g) dissolved in methylene chloride (50 ml) was added (carbomethoxymethylene)triphenylphosphorane (6.75 g), and the mixture was stirred for 4 hours. Then, the reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.91 g). The product was dissolved in acetonitrile (30 ml), and 1M tetra-n-butylammonium chloride in THF (27 ml) and potassium fluoride (7.6 g) were added. The mixture was heated under reflux for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexaneethylacetate 100:1 to give the methyl ester of 14-fluoro-3-tetradecenoic acid (3.3 g). Then, the reaction mixture was concentrated the residue thus obtained

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromo-1-dodecanol (5 g) dissolved in methylene chloride (70 ml) were added pyridinium chlorochromate (10.1 g) and Celite (11.0 g), and the mixture was stirred at room temperature for 12 hours. Then, the reaction mixture was filtered, concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (20:1 ) to give 12-bromo-1-dodecanal (3.72 g). To the product dissolved in methylene chloride (50 ml ) was added (carbomethoxymethylene)triphenylphosphorane (8.80 g), and the mixture was stirred. The reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (20:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.14 g). The product was dissolved in methanol and stirred under hydrogen atmosphere in the presence of palladium/carbon (1.5 g) for 18 hours. The reaction mixture was filtered and concentrated to give the methyl ester of 14-bromotetradecanoic acid (3.35 g). 50% Aqueous ethanol (100 ml), in which potassium hydroxide (2.90 g) had been dissolved, was added to the methyl ester, and the mixture was stirred at 60° C. for 1 hour. Ethanol in the reaction mixture was removed by distillation, and the residue was acidified to a weak acidic range of pH by adding citric acid and extracted with ethyl acetate. The organic layer was dried and concentrated to give 14-bromotetradecanoic acid (3.55 g). After the product was dissolved in N,N-dimethylformamide (DMF, 50 ml), para-nitrophenol (1.61 g) and N,N'-dicyclohexylcarbodiimide (2.39 g) were added, and the mixture was stirred for 12 hours. Then, precipitates produced was removed by filtration and the DMF was removed by distillation. The residue was subjected to chromatography on a silica gel column with eluent systems of n-hexane-ethyl acetate (from 200:1 to 50:1) to give the active ester of 14-bromotetradecanoic acid (2.57 g). The active ester (655 mg) was dissolved in DMF (30 ml), and 6-(4'-N-glycyl-spicaminyl-amino)purine hydrochloride (500 mg) and triethylamine (2.0 ml) were added to the solution. The mixture was stirred for 12 hours. After the solvent was removed by distillation, the residue was subjected to chromatography on a silica gel column with eluent systems of chloroform-methanol (from 7:1 to 5:1) to give SPK273 in the yield of 219 mg. Then, the reaction mixture was filtered concentrated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromo-1-dodecanol (5 g) dissolved in methylene chloride (70 ml) were added pyridinium chlorochromate (10.1 g) and Celite (11.0 g), and the mixture was stirred at room temperature for 12 hours. Then, the reaction mixture was filtered, concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (20:1 ) to give 12-bromo-1-dodecanal (3.72 g). To the product dissolved in methylene chloride (50 ml ) was added (carbomethoxymethylene)triphenylphosphorane (8.80 g), and the mixture was stirred. The reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (20:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.14 g). The product was dissolved in methanol and stirred under hydrogen atmosphere in the presence of palladium/carbon (1.5 g) for 18 hours. The reaction mixture was filtered and concentrated to give the methyl ester of 14-bromotetradecanoic acid (3.35 g). 50% Aqueous ethanol (100 ml), in which potassium hydroxide (2.90 g) had been dissolved, was added to the methyl ester, and the mixture was stirred at 60° C. for 1 hour. Ethanol in the reaction mixture was removed by distillation, and the residue was acidified to a weak acidic range of pH by adding citric acid and extracted with ethyl acetate. The organic layer was dried and concentrated to give 14-bromotetradecanoic acid (3.55 g). After the product was dissolved in N,N-dimethylformamide (DMF, 50 ml), para-nitrophenol (1.61 g) and N,N'-dicyclohexylcarbodiimide (2.39 g) were added, and the mixture was stirred for 12 hours. Then, precipitates produced was removed by filtration and the DMF was removed by distillation. The residue was subjected to chromatography on a silica gel column with eluent systems of n-hexane-ethyl acetate (from 200:1 to 50:1) to give the active ester of 14-bromotetradecanoic acid (2.57 g). The active ester (655 mg) was dissolved in DMF (30 ml), and 6-(4'-N-glycyl-spicaminyl-amino)purine hydrochloride (500 mg) and triethylamine (2.0 ml) were added to the solution. The mixture was stirred for 12 hours. After the solvent was removed by distillation, the residue was subjected to chromatography on a silica gel column with eluent systems of chloroform-methanol (from 7:1 to 5:1) to give SPK273 in the yield of 219 mg. Then, the reaction mixture was filtered concentrated

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 1-bromopentane (2.54 ml, 20.51 mmol) in THF (5 ml) was added dropwise to a stirred suspension of Mg metal (0.54 g, 22.23 mmol) and a catalytic amount of iodine in dry THF (15 ml) at 75° C., after which stirring was continued for another 30 minutes. The generated Grignard reagent was cooled to room temperature and added slowly to a stirred solution of 12-bromododecanal (4.5 g, 17.09 mmol) in THF (40 ml) at 0° C. The reaction was warmed to room temperature and stirring continued another 1.5 hours, then quenched with NH4Cl solution, and extracted with EtOAc (3×50 ml). The combined organic layers were washed with brine solution, dried on MgSO4 and concentrated. The crude compound was purified over silica gel column (8% EtOAc in hexane) to give 17-bromoheptadecan-6-ol as an off-white low melting solid (3.34 g, 58%). continued another 1.5 hours quenched with NH4Cl solution extracted with EtOAc (3×50 ml) The combined organic layers were washed with brine solution dried on MgSO4 concentrated The crude compound was purified over silica gel column (8% EtOAc in hexane)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 1-bromopentane (2.54 ml, 20.51 mmol) in THF (5 ml) was added dropwise to a stirred suspension of Mg metal (0.54 g, 22.23 mmol) and a catalytic amount of iodine in dry THF (15 ml) at 75° C., after which stirring was continued for another 30 minutes. The generated Grignard reagent was cooled to room temperature and added slowly to a stirred solution of 12-bromododecanal (4.5 g, 17.09 mmol) in THF (40 ml) at 0° C. The reaction was warmed to room temperature and stirring continued another 1.5 hours, then quenched with NH4Cl solution, and extracted with EtOAc (3×50 ml). The combined organic layers were washed with brine solution, dried on MgSO4 and concentrated. The crude compound was purified over silica gel column (8% EtOAc in hexane) to give 17-bromoheptadecan-6-ol as an off-white low melting solid (3.34 g, 58%). continued another 1.5 hours quenched with NH4Cl solution extracted with EtOAc (3×50 ml) The combined organic layers were washed with brine solution dried on MgSO4 concentrated The crude compound was purified over silica gel column (8% EtOAc in hexane)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 1-bromopentane (2.54 ml, 20.51 mmol) in THF (5 ml) was added dropwise to a stirred suspension of Mg metal (0.54 g, 22.23 mmol) and a catalytic amount of iodine in dry THF (15 ml) at 75° C., after which stirring was continued for another 30 minutes. The generated Grignard reagent was cooled to room temperature and added slowly to a stirred solution of 12-bromododecanal (4.5 g, 17.09 mmol) in THF (40 ml) at 0° C. The reaction was warmed to room temperature and stirring continued another 1.5 hours, then quenched with NH4Cl solution, and extracted with EtOAc (3×50 ml). The combined organic layers were washed with brine solution, dried on MgSO4 and concentrated. The crude compound was purified over silica gel column (8% EtOAc in hexane) to give 17-bromoheptadecan-6-ol as an off-white low melting solid (3.34 g, 58%). continued another 1.5 hours quenched with NH4Cl solution extracted with EtOAc (3×50 ml) The combined organic layers were washed with brine solution dried on MgSO4 concentrated The crude compound was purified over silica gel column (8% EtOAc in hexane)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 12-bromododecanol (5 g) dissolved in methylene chloride (30 ml) were added Celite (5.0 g) and pyridinium chlorochromate (5.2 g), and the mixture was stirred at room temperature for 12 hours. Then, the reaction mixture was filtered and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give 12-bromododecanal (4.4 g). To 12-bromododecanal (4.4 g) dissolved in methylene chloride (50 ml) was added (carbomethoxymethylene)-triphenylphosphorane (6.75 g), and the mixture was stirred for 4 hours. Then, the reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.91 g). The product was dissolved in acetonitrile (30 ml), and 1M tetra-n-butylammonium chloride in THF (27 ml) and potassium fluoride (7.6 g) were added. The mixture was heated under reflux for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethylacetate 100:1 to give the methyl ester of 14-fluoro-3-tetradecenoic acid (3.3 g). Then, the reaction mixture was concentrated the residue thus obtained