戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2222983作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物O-benzotriazol-1-yl-tetramethyluroniumHCID 130500—
反応物Benzyloxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acidHCID 68798586—
反応物2-((S)-2-amino-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl esterHCID 86604040—
溶媒DimethylformamideHCID 6228—
生成物2-{(S)-2-[2-benzyloxycarbonylamino-2-(4-methoxy-3-methyl-phenyl)-acetylamino]-3-phenyl-propionylamino}-thiazole-4-carboxylic acid methyl esterHCID 8660405869.3%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07371869B2
出典データセットuspto-grants-2008_05
ORD IDord-4b1de5cdc0af479d9c55e082234a0818
出典メモuspto-grants-2008_05