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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 659686생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/659686

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-Bromo-1H-imidazoleHCID 2773261—
반응물3-(3-Bromomethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamideHCID 67003981—
용매Dimethyl SulfoxideHCID 679—
용매DichloromethaneHCID 6344—
생성물3-[3-(2-bromoimidazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamideHCID 6713297199%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08080571B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-65988bf132aa4dc887dfc212dc2bf758
출처 메모uspto-grants-2011_12