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HRID 1665022作成日:2026年10月26日

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

https://huagongshe.com/reaction/1665022

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Cesium carbonateHCID 10796—
反応物2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamideHCID 67439913—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物N-benzyl-2-chloro-N-[2-(3-methanesulfonyl-phenyl)-thiazol-5-ylmethyl]-benzenesulfonamideHCID 25234386—

反応手順

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]+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08039493B2
出典データセットuspto-grants-2011_10
ORD IDord-83a7a06b6d6a496b9ffd9744c62736d4
出典メモuspto-grants-2011_10