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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677217생성일: 2026년 10월 25일

Bromotrimethylsilane → (1S,5S)-(1-{5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-phosphonooxy hexylcarbamoyl}-2,2-diphenyl-ethyl)-carbamic acid methyl ester

https://huagongshe.com/reaction/1677217

반응식

참여 물질

역할이름HCID투입량
반응물BromotrimethylsilaneHCID 76113—
반응물(1S,5S)-{1-[5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-(diethoxy-phosphoryloxy)-hexylcarbamoyl]-2,2-diphenyl-ethyl}-carbamic acid methyl esterHCID 24778259—
용매DichloromethaneHCID 6344—
생성물(1S,5S)-(1-{5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-phosphonooxy hexylcarbamoyl}-2,2-diphenyl-ethyl)-carbamic acid methyl esterHCID 11563875—

반응 단계

The product of step G prepared above (152 mg) was dissolved in anhydrous dichloromethane (3.0 mL). Trimethylsilyl bromide (0.5 mL) was added at 0° C. The mixture was stirred during 1 h at this temperature and overnight at room temperature. The solvent was evaporated and 0.2 mL water was added to the residue. 3 mL EtOH was added mixed and evaporated. This step was repeated three times and the residue dried in vacuo. Yields 98 mg 70% of the title derivatives of this first example.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008297B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-d278040c535142fb99d6db8f853bbedb
출처 메모uspto-grants-2011_08