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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73853생성일: 2026년 10월 24일

1-Hydroxybenzotriazole → 1-[(2-Benzothienylcarbonyl)amino]cyclohexanecarboxylic acid phenylmethyl ester

https://huagongshe.com/ko/reaction/73853

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Benzo(b)thiophene-2-carboxylic acidHCID 95864—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Benzyl 1-aminocyclohexanecarboxylateHCID 15176238—
용매DichloromethaneHCID 6344—
생성물1-[(2-Benzothienylcarbonyl)amino]cyclohexanecarboxylic acid phenylmethyl esterHCID 5767289791%

반응 단계

Under ice-cooling, 5.9 g (31 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added to a solution of 5 g (28 mmol) of 2-benzothiophenecarboxylic acid, 6.5 g (28 mmol) of 1-aminocyclohexanecarboxylic acid phenylmethyl ester and 4.5 g (29 mmol) of 1-hydroxybenzotriazole in methylene chloride. After the mixture was stirred at room temperature overnight, the reaction solvent was distilled off under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate twice. The obtained organic layer was washed with a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and then saturated brine, and it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, diethyl ether was added to the obtained residue, and the mixture was stirred overnight. The crystal was collected by filtration and heated/dried under reduced pressure to obtain 10 g (91%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829209B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3f8e2bf61c354e568d0daf7c0bd00327
출처 메모uspto-grants-2014_09