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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29192생성일: 2026년 10월 23일

Dimethylformamide → tert-Butyl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy) (2-[(methoxycarbonyl)amino]benzimidazol-5-ylsulfonyl)amino-2-hydroxypropyl)carbamate

https://huagongshe.com/ko/reaction/29192

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Methyl N-[6-(chlorosulfonyl)-1H-benzimidazol-2-yl]carbamateHCID 15124047—
반응물tert-Butyl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)amino-2-hydroxypropyl)carbamateHCID 21356391—
반응물DiisopropyldiethylamineHCID 21936557—
용매Ethyl AcetateHCID 8857—
생성물tert-Butyl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy) (2-[(methoxycarbonyl)amino]benzimidazol-5-ylsulfonyl)amino-2-hydroxypropyl)carbamateHCID 86585040—

반응 단계

tert-Butyl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)amino-2-hydroxypropyl)carbamate (step 1, Example 54), (0.75 g, 2.1 mmol) was combined with 2-(methoxycarbonyl)amino benzimidazol-5-ylsulfonyl chloride (0.89 g, 3.1 mmol) in anhydrous DMF (15 ml) under a N2 atmosphere. Diisopropylethylethyl amine (1.08 ml, 6.2 mmol) was added and the reaction was stirred at room temperature for 24 hours. The reaction mixture was diluted in EtOAc and washed with sat. NaHCO3, 0.5N KHSO4 and brine. Organic phase was dried with MgSO4 and solvent was removed in vacuo. Purification by flash chromatography (CH2Cl2 to 1% MeOH in CH2Cl2 to 2% to 3% to 4%). Recovered 0.79 g (62%) of product as a white foam. Rf=0.08 (3% MeOH/CH2Cl2). HPLC tR=10.47 min (C18 column). LRMS (M+H)+ 618.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419967B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-80392b89ee484fe3b98243eddcccd240
출처 메모uspto-grants-2008_09