돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1696639생성일: 2026년 10월 24일

Sodium hydride → 2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehyde

https://huagongshe.com/ko/reaction/1696639

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-MercaptobenzimidazoleHCID 707035—
반응물2-Chloro-1,3-thiazole-5-carbaldehydeHCID 1479765—
용매TetrahydrofuranHCID 8028—
생성물2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehydeHCID 5982574670.7%

반응 단계

1,3-Dihydro-benzimidazole-2-thione (1.0 g, 6.66 mmol) is suspended into 50 mL of tetrahydrofuran under argon. Then, 479 mg (9.99 mmol) of sodium hydride is added. The reaction mixture is stirred at room temperature until gas evolution has ceased. 2-Chloro-1,3-thiazole-5-carbaldehyde (983 mg, 6.66 mmol) is then added and the reaction mixture is stirred at room temperature for 2 h, upon which it is filtered. The solid is washed with tetrahydrofuran and dried under reduced pressure. The residue is diluted with water and extracted twice with ethyl acetate and once with dichloromethane. The organic extracts are combined, dried on magnesium sulfate, filtered and concentrated under reduced pressure. 1.23 g of 2-(1H-benzimidazol-2-ylsulfanyl)-thiazole-5-carbaldehyde is obtained as a pale yellow powder. mp: 188° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163768B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-8774921c530b4d5aabd29eb07c113f19
출처 메모uspto-grants-2012_04