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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2222983생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → 2-{(S)-2-[2-benzyloxycarbonylamino-2-(4-methoxy-3-methyl-phenyl)-acetylamino]-3-phenyl-propionylamino}-thiazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2222983

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물O-benzotriazol-1-yl-tetramethyluroniumHCID 130500—
반응물Benzyloxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acidHCID 68798586—
반응물2-((S)-2-amino-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl esterHCID 86604040—
용매DimethylformamideHCID 6228—
생성물2-{(S)-2-[2-benzyloxycarbonylamino-2-(4-methoxy-3-methyl-phenyl)-acetylamino]-3-phenyl-propionylamino}-thiazole-4-carboxylic acid methyl esterHCID 8660405869.3%

반응 조건

온도0 °C

반응 단계

To a solution of 2-((S)-2-amino-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl ester (0.93 g, 3.04 mmol), benzyloxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid (1.0 g, 3.04 mmol), diisopropylethylamine (2.1 mL, 12 mmol) and 1-hydroxybenzotriazole (0.46 g, 3.04 mmol) in N,N-dimethylformamide (10 mL) at 0° C. was added O-benzotriazol-1-yl-N,N, N′,N′-tetramethyluronium hexaflurorophosphate (1.15 g, 3.04 mmol). The reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was separated, washed with water, brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography over silica gel eluted with 2:1 ethyl acetate/hexanes to give 2-{(S)-2-[2-benzyloxycarbonylamino-2-(4-methoxy-3-methyl-phenyl)-acetylamino]-3-phenyl-propionylamino}-thiazole-4-carboxylic acid methyl ester as a white solid (1.3 g, 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07371869B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-4b1de5cdc0af479d9c55e082234a0818
출처 메모uspto-grants-2008_05