methyl piperazine-1-carboxylate;hydrochloride

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo

Conditions: temp:79.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1. The resulting reaction mixture to cool to RT The organic layer was extracted with 1 M HCl (3×20 mL) the combined aqueous layers were treated with 3 N NaOH until the pH=10 The resulting solution was extracted three times with EtOAc the combined organic layers were dried over sodium sulfate filtered concentrated in vacuo