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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501592생성일: 2026년 10월 24일

Acetic Acid → (2R,3R)-N-tert-Butyloxycarbonyl-3-(tert-butyldimethylsiloxy)-2-[(3-chloro-4-cyano-2-methylphenylamino)methyl]pyrrolidine

https://huagongshe.com/ko/reaction/501592

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물tert-Butyl-(2S,3R)-3-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpyrrolidine-1-carboxylateHCID 16732142—
반응물4-Amino-2-chloro-3-methylbenzonitrileHCID 21875413—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물(2R,3R)-N-tert-Butyloxycarbonyl-3-(tert-butyldimethylsiloxy)-2-[(3-chloro-4-cyano-2-methylphenylamino)methyl]pyrrolidineHCID 5942484163%

반응 단계

To a solution of (2S,3R)-3-(tert-Butyldimethylsilanyloxy)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (51C) (661 mg, 2.0 mmol) in 5% DMF in CH2Cl2 (10 mL) at rt was added 4-amino-2-chloro-3-methyl-benzonitrile (340 mg, 2.04 mmol) followed by NaBH(OAc)3 (636 mg, 3.0 mmol) and HOAc (180 μL, 3 mmol). The reaction was stirred under nitrogen at rt for 18 h. Additional portions of NaBH(OAc)3 (424 mg, 2.0 mmol) and HOAc (120 μL, 2 mmol) were added, and the reaction was stirred for an additional 18 h. The reaction was diluted with EtOAc (50 mL) and the organic layer was washed with saturated aqueous NaHCO3 (50 ml), dried (MgSO4), filtered and concentrated. Purification via flash chromatography (silica gel, 0 to 15% EtOAc/hexanes) provided the title compound (605 mg, 1.26 mmol, 63%). MS m/z 480 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772267B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-182c28df328b40b69754c4df7d5a5fb1
출처 메모uspto-grants-2010_08