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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1665022생성일: 2026년 10월 26일

Benzyl Bromide → N-benzyl-2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamide

https://huagongshe.com/reaction/1665022

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Cesium carbonateHCID 10796—
반응물2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamideHCID 67439913—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물N-benzyl-2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamideHCID 25234386—

반응 단계

To a stirred solution of 2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamide (30 mg) in N,N-dimethylacetamide (0.6 mL) were added benzyl bromide (13 mg) and cesium carbonate (26 mg). The mixture was stirred overnight at r.t. The mixture was diluted with ethyl acetate and washed with water. The organic phase was dried (MgSO4), filtered and concentrated under reduced pressure. The product was purified by chromatography (SiO2, cyclohexane/ethyl acetate 1:0 to 1:1) to give N-benzyl-2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamide as a colorless solid. MS: 534.8 ([M+H]+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08039493B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-83a7a06b6d6a496b9ffd9744c62736d4
출처 메모uspto-grants-2011_10