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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1264638생성일: 2026년 10월 26일

Methyl 2-cyano-3,3-bis(methylsulfanyl)prop-2-enoate → 2-Cyano-3-[[(3S)-hexahydro-2-oxo-1-[2-oxo-2-(1-pyrrolidinyl)ethyl]-1H-azepin-3-yl]amino]-3-[(2-methyl-6-benzofuranyl)amino]propenoic acid methyl ester

https://huagongshe.com/reaction/1264638

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2-cyano-3,3-bis(methylsulfanyl)prop-2-enoateHCID 319957—
반응물(S)-1-[(3-amino-hexahydro-2-oxo-1H-azepin-1-yl)acetyl]pyrrolidineHCID 12047820—
반응물2-Methyl-1-benzofuran-6-amineHCID 18612539—
용매AcetonitrileHCID 6342—
생성물2-Cyano-3-[[(3S)-hexahydro-2-oxo-1-[2-oxo-2-(1-pyrrolidinyl)ethyl]-1H-azepin-3-yl]amino]-3-[(2-methyl-6-benzofuranyl)amino]propenoic acid methyl esterHCID 7003021411%

반응 단계

In a procedure similar to that in example 36, the title compound (8 mg, 11%) was synthesized from 2-methyl-6-benzofuranamine (34 mg, 0.23 mmol), methyl 2-cyano-3,3-bis(methylthio)-2-propenoate (47 mg, 0.23 mmol), and 1-[[(3S)-3-aminohexahydro-2-oxo-1H-azepin-1-yl]acetyl]pyrrolidine (102 mg, 0.43 mmol) using acetonitrile as the reaction solvent: MS (ESI, pos, ion) m/z 494 (M+H); HPLC (method C) tR 3.6 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06544981B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-47b1c1df66fe4d6a9636855aad5b5f0b
출처 메모uspto-grants-2003_04