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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432952생성일: 2026년 10월 25일

Sulfuric Acid → (6R-trans)-1-chloro-N-[2-chloro-4-fluoro-5-(tetrahydro-6-hydroxy-1,3-dioxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl)phenyl]methanesulfonamide

https://huagongshe.com/reaction/432952

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참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물(2R-cis)-1-[[[4-chloro-5-[[(chloromethyl)sulfonyl]amino]-2-fluorophenyl]amino]carbonyl]4-hydroxy-2-pyrrolidinecarboxylic acidHCID 53809153—
용매Methyl Isobutyl KetoneHCID 7909—
생성물(6R-trans)-1-chloro-N-[2-chloro-4-fluoro-5-(tetrahydro-6-hydroxy-1,3-dioxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl)phenyl]methanesulfonamideHCID 1098251388.9%

반응 조건

온도0 °C

반응 단계

295.5 g (0.25 mol) of (2R-cis)-1-[[[4-chloro-5-[[(chloromethyl)sulfonyl]amino]-2-fluorophenyl]amino]carbonyl]-4-hydroxy-2-pyrrolidinecarboxylic acid was suspended in 150 g of methyl isobutyl ketone at room temperature. 12.75 g (0.125 mol) of concentrated sulfuric acid was added and the clear solution was heated to reflux. At 90° C. a precipitate appeared. After an additional 20 minutes of stirring at reflux the suspension was cooled to 0° C. and allowed to stir for 1 hour at this temperature. After filtration and drying at 60° C., 91.65 g (86.6%) of the title compound was obtained as beige crystals melting at 198-200° C. (purity: 97%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664400B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-5326204c9d474a91bb878307a3b51a55
출처 메모uspto-grants-2003_12