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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10997생성일: 2026년 10월 24일

p-(Trifluoromethoxy)benzenesulphonyl chloride → CID 145857204

https://huagongshe.com/ko/reaction/10997

반응식

참여 물질

역할이름HCID투입량
반응물p-(Trifluoromethoxy)benzenesulphonyl chlorideHCID 523102—
반응물tert-butyl N-[4-[[[(6S)-3-(methanesulfonamido)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamateHCID 145857232—
반응물tert-butyl N-[4-[[[(6S)-3-(diethylamino)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamateHCID 145857233—
생성물CID 145857204HCID 14585720441.6%

반응 단계

Following a procedure similar to that for the preparation of 16a, intermediate 3a (50 mg, 0.117 mmol) and 4-(trifluoromethoxy)benzene sulfonyl chloride (39.6 mg, 0.152 mmol) yielded 31.7 mg (41.6%) of 33a. MS (ESI) 651.0 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094783B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4c34701dba374642a831397d727793bd
출처 메모uspto-grants-2006_08