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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645422생성일: 2026년 10월 27일

Diisopropylcarbodiimide → 4-[4-[[(Phenylmethoxy)amino]carbonyl]phenyl]-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/645422

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물Benzyloxyamine hydrochlorideHCID 102312—
반응물4-[4-(tert-Butoxycarbonyl)piperazin-1-yl]benzoic acidHCID 2795508—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물4-[4-[[(Phenylmethoxy)amino]carbonyl]phenyl]-1-piperazinecarboxylic acid, 1,1-dimethylethyl esterHCID 86598201104%

반응 단계

A mixture of 4-(4-carboxyphenyl)-1-piperazinecarboxylic acid, 1-(1,1-dimethylethyl) ester (0.032 mol), O-(phenylmethyl)-hydroxylamine hydrochloride (0.064 mol), DMAP (0.03 mol) in DCM p.a. (250 ml) and TEA (14 ml) was stirred at room temperature. DIC (0.064 mol) was added. The reaction mixture was stirred at room temperature for 8 hours, then washed with water, HCl (0.5N) and water. The separated organic layer was dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: DCM/MeOH 98/2). The desired fractions were collected and the solvent was evaporated, yielding 13.7 g of 4-[4-[[(phenylmethoxy)amino]carbonyl]phenyl]-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester (interm. 4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07704998B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-02cf36fcf8d04acd86d6f9e6dc0082d1
출처 메모uspto-grants-2010_04