戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 659686作成日:2026年10月26日

Sodium Hydroxide → 3-[3-(2-bromoimidazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide

https://huagongshe.com/reaction/659686

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2-Bromo-1H-imidazoleHCID 2773261—
反応物3-(3-Bromomethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamideHCID 67003981—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
生成物3-[3-(2-bromoimidazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamideHCID 6713297199%

反応手順

To a solution of 2-bromoimidazole (68.9 mg, 0.469 mmol; see step (a)) in DMSO (1 mL) and NaOH (32.8 mg, 0.82 mmol), that had been stirred for 40 min at ambient temperature, was added a solution of 3-(3-bromomethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (173.6 mg, 0.391 mmol; see Example 1(e)) in DMSO (1 mL) dropwise. The reaction mixture was stirred for 1 h at ambient temperature and then diluted with CH2Cl2 (15 mL). The organic layer was washed with water, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue purified by flash chromatography using MeOH:CH2Cl2 (3:97) as eluent to give the sub-title compound in 99% yield as a colourless syrup (197.3 mg, 0.387 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08080571B2
出典データセットuspto-grants-2011_12
ORD IDord-65988bf132aa4dc887dfc212dc2bf758
出典メモuspto-grants-2011_12