N,N-dimethylpent-2-yn-1-amine

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 a cooled solution of 2-Methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylamine (29 mg, 0.13 mmol) in 2.4 mL of dichloromethane were added 0.11 mL (0.66 mmol) of diisopropylethylamine and 78 uL of a 20% solution of phosgene in toluene at 0 C. The reaction mixture was stirred at 0 C for 20 minutes and transferred into a flask containing 140 mg (18% pure, 0.17 mmol) of dimethyl-pent-2-ynylamine. The reaction mixture was stirred at RT for 18 hour then applied to column chromatography without workup. Chromatography (0->50% in hexanes/ethyl acetate in 30 minutes) gave 27 mg (73 umol, 60%) of the title compound. transferred into a flask The reaction mixture was stirred at RT for 18 hour

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To an ice cold solution of 1-dimethylamino-2-pentyne (3.0 g) in dichioromethane (100 ml) was added 3-chloroperoxybenzoic acid (4.66 g) in small portions. After the reaction was stirred at 0° C. for 20 minutes, the mixture was passed over twenty weight equivalents of basic alumina (Brockmann Grade I, 150 mesh) and the N-oxide was eluted using a solution of 5% methanol in dichloromethane. All fractions containing 1-dimethylamino-2-pentyne N-oxide were combined and evaporated to near dryness in vacuo. The residue was treated successively three times with of methanol (ca. 100 ml) followed by evaporation to near dryness, and the volume of the solution was adjusted to 90 mL by addition of methanol. One third of this methanolic solution (30 ml) of the N-oxide (9 mmol) was heated to reflux for approximately 4 hours, cooled, evaporated to dryness in vacuo, and the residue was chromatographed over silica gel (2% methanol in dichloromethane was used as the eluant) to give upon evaporation of the solvent in vacuo the desired product as an oil. MS (+ES) m/z: 128 (M+H)+ the N-oxide was eluted All fractions containing 1-dimethylamino-2-pentyne N-oxide evaporated The residue was treated successively three times with of methanol (ca. 100 ml) followed by evaporation the volume of the solution was adjusted to 90 mL by addition of methanol to reflux for approximately 4 hours cooled evaporated to dryness in vacuo the residue was chromatographed over silica gel (2% methanol in dichloromethane