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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216945생성일: 2026년 10월 26일

Methyl N-(triethylammoniosulfonyl)carbamate → (S)-tert-Butyl 4-(1-cyano-2-(3'-cyano-4'-methylbiphenyl-4-yl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216945

반응식

참여 물질

역할이름HCID투입량
반응물Methyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
반응물(S)-tert-Butyl 4-(1-amino-3-(3'-cyano-4'-methylbiphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568611—
용매DichloromethaneHCID 6344—
생성물(S)-tert-Butyl 4-(1-cyano-2-(3'-cyano-4'-methylbiphenyl-4-yl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 5956855985.5%

반응 단계

(S)-tert-Butyl 4-(1-amino-3-(3′-cyano-4′-methylbiphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 18, step (i), 154 mg) in dichloromethane (8 mL) was treated with Burgess' reagent (145 mg) and the mixture was stirred at room temperature for 18 h. The solvent was partially evaporated and the mixture was purified by chromatography on silica eluting with ethyl acetate/isohexane (1:1) to afford the sub-titled compound (127 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193239B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-511794996dd44379ac3413d7181e3d40
출처 메모uspto-grants-2012_06