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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219612생성일: 2026년 10월 24일

HCID 88542676, 화합물 → tert-butyl (S)-1-(4-bromophenyl)ethyl((S)-4-((R)-1,1-dimethylethylsulfinamido)-6-methyl-4-phenylhept-6-enyl)carbamate

https://huagongshe.com/ko/reaction/219612

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참여 물질

역할이름HCID투입량
반응물HCID 88542676HCID 88542676—
반응물HCID 178448200HCID 178448200—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl (S)-1-(4-bromophenyl)ethyl((S)-4-((R)-1,1-dimethylethylsulfinamido)-6-methyl-4-phenylhept-6-enyl)carbamateHCID 67986476—

반응 단계

A solution of tert-butyl (S)-1-(4-bromophenyl)ethyl((E)-4-((R)-tert-butylsulfinylimino)-4-phenylbutyl)carbamate (1.97 g, 3.59 mmol) in dry THF (60 mL) was cooled to −78° C. A solution of 2-methylallylmagnesium chloride (0.5M in THF, 14.4 mL, 2 equiv) was added slowly. After 2 h, the mixture was warmed to rt and stirred for 1 h. LC-MS found reaction completed. The mixture was quenched with satd aq NH4Cl (10 mL), diluted with ether (100 mL), washed with water (30 mL), brine (25 mL), dried over Na2SO4. Filtration and concentration gave crude tert-butyl (S)-1-(4-bromophenyl)ethyl((S)-4-((R)-1,1-dimethylethylsulfinamido)-6-methyl-4-phenylhept-6-enyl)carbamate (2.30 g) which was used for next steps without further purifications. LC-MS Method 1 tR=2.53 min, m/z 605, 607(M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202857B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-c8aff95c99b042608a1ab693a9689c76
출처 메모uspto-grants-2012_06