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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50030생성일: 2026년 10월 24일

L-(+)-Cysteine → (2R)-2-amino-3-{[2-(5-methyl-4-oxo-5-phenyl-4,5-dihydrofuran-2-yl)-1-thien-3-ylethyl]thio}propanoic acid

https://huagongshe.com/ko/reaction/50030

반응식

참여 물질

역할이름HCID투입량
반응물L-(+)-CysteineHCID 5862—
반응물(E)-2-methyl-2-phenyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanoneHCID 11300541—
생성물(2R)-2-amino-3-{[2-(5-methyl-4-oxo-5-phenyl-4,5-dihydrofuran-2-yl)-1-thien-3-ylethyl]thio}propanoic acidHCID 10179320—

반응 단계

Following the procedure of Method C, Example 1, (E)-2-methyl-2-phenyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone was reacted with L-cysteine to provide (2R)-2-amino-3-{[2-(5-methyl-4-oxo-5-phenyl-4,5-dihydrofuran-2yl)-1-thien-3-ylethyl]thio}propanoic acid: 1H NMR (DMSO-d6) δ1.50-1.60 (overlapping singlets, 3H), 2.70-3.10 (m, ˜2H), 4.00-4.25 (m, 1H), 4.64 (m, 1H), 5.50-5.57 (overlapping singlets, 1H), 7.12-7.38 (m, 6H), 7.52-7.63 (m, 2H), 8.35 (br s, ˜2H); MS (LR-ESI) m/z 402 (M-H calcd. for C20H20NO4S2 402)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710078B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d790d9abdbae4f89bc5f814f6b774d13
출처 메모uspto-grants-2004_03