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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2304135생성일: 2026년 10월 27일

Triethylamine → 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(4,5,6,7-tetrahydrobenzothiazol-2-yl)-propionamide

https://huagongshe.com/reaction/2304135

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Amino-4,5,6,7-tetrahydrobenzothiazoleHCID 18046—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(4,5,6,7-tetrahydrobenzothiazol-2-yl)-propionamideHCID 1201054279%

반응 단계

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (50 mg, 0.17 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (83 mg, 0.19 mmol), triethylamine (0.048 mL, 0.34 mmol), and 2-amino-4,5,6,7-tetrahydrobenzothiazole (40 mg, 0.26 mmol) in dry N,N-dimethylformamide (1 mL) was stirred at 25° C. for 14 h. The reaction mixture was then diluted with water and ethyl acetate, and the layers were separated. The organic layer was sequentially washed with a 1N aqueous hydrochloric acid solution, a saturated aqueous sodium chloride solution, and water. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(4,5,6,7-tetrahydrobenzothiazol-2-yl)-propionamide (56 mg, 79%) as a white solid: mp 170-171° C.; EI-HRMS m/e calcd for C21H24Cl2N2OS (M+) 422.0986, found 422.0982.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06433188B1
출처 데이터셋uspto-grants-2002_08
ORD IDord-f90dc5a5c21f42acb7b38622853dacb1
출처 메모uspto-grants-2002_08