反应 #543600

ord-ebce91a0bdcf4747af517199af5f5467

反应方程式

COc1ccc(C(=O)CCC(=O)N2CCN3CCC[C@H]3C2)cc1OC
1-(3,4-dimethoxyphenyl)-4-((S)-hexahydropyrrolo[1,2-a]pyrazin-2-yl)butane-1,4-dione
CC(C)(C)OC(=O)N1CCCC[C@@H]1C(=O)O
(R)-1-(tert-butoxycarbonyl)piperidine 2 carboxylic acid
COc1ccc(C(=O)CCC(=O)O)cc1F
3-(3-fluoro-4-methoxybenzoyl)propionic acid
COc1ccc(C(=O)CCC(=O)N2CCN3CCCC[C@@H]3C2)cc1F
title compound
COc1ccc(C(=O)CCC(=O)N2CCN3CCCC[C@@H]3C2)cc1F
1-(3-Fluoro-4-methoxyphenyl)-4-((R)-octahydropyrido[1,2-a]pyrazin-2-yl)butane-1,4-dione

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

93 mg of the title compound were prepared as described for 1-(3,4-dimethoxyphenyl)-4-((S)-hexahydropyrrolo[1,2-a]pyrazin-2-yl)butane-1,4-dione, using (R)-1-(tert-butoxycarbonyl)piperidine 2 carboxylic acid instead of BOC-protected proline and 3-(3-fluoro-4-methoxybenzoyl)propionic acid instead of 3-(3,4-dimethoxybenzoyl)propionic acid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186721B2uspto-grants-2007_03