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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1871729생성일: 2026년 10월 27일

Tetrachlorocatechol → (R)-1-[[2-[2-[(R)-2-tert-butoxycarbonyl-pyrrolidin-1-yl]-2-oxo-ethoxy]-3,4,5,6-tetrachloro-phenoxy]-acetyl]-pyrrolidine-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1871729

반응식

참여 물질

역할이름HCID투입량
반응물TetrachlorocatecholHCID 14537—
반응물Potassium tert-butoxideHCID 23665647—
반응물Bromoacetyl-pyrrolidine-2-carboxylic acid tert-butyl esterHCID 70037232—
용매DimethylformamideHCID 6228—
생성물(R)-1-[[2-[2-[(R)-2-tert-butoxycarbonyl-pyrrolidin-1-yl]-2-oxo-ethoxy]-3,4,5,6-tetrachloro-phenoxy]-acetyl]-pyrrolidine-2-carboxylic acid tert-butyl esterHCID 5421551045%

반응 단계

To a solution of 185 mg (1.65 mmol) potassium tert-butylate in 1 ml dimethylformamide at room temperature was added dropwise a solution of 186 mg (0.75 mmol) tetrachlorocatechol in 1 ml dimethylformamide. Stirring was continued for 2-3 min and a solution of 438 mg (1.50 mmol) (R)-(1) -bromoacetyl-pyrrolidine-2-carboxylic acid tert-butyl ester in 2 ml dimethylformamide was added within 1-2 min. The reaction mixture was stirred for additional 4 h at room temperature. The solvent was removed in vacuo and the residue purified by flash-chromatography to yield 229 mg (45%) of the title compound as a white foam. MS m/e (%): 671 (M+H+, 100), 615 (19), 559 (14).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06103910
출처 데이터셋uspto-grants-2000_08
ORD IDord-8440744a0f3447d3b46c4f0f0cb923c7
출처 메모uspto-grants-2000_08