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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 912678생성일: 2026년 10월 26일

Benzoyl isothiocyanate → 1-[2-(1H-Benzimidazol-2-yl)ethyl]thiourea

https://huagongshe.com/reaction/912678

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl isothiocyanateHCID 68284—
반응물DiisopropylethylamineHCID 81531—
반응물Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
반응물2-(1H-Benzimidazol-2-yl)ethan-1-amineHCID 415158—
용매DichloromethaneHCID 6344—
생성물1-[2-(1H-Benzimidazol-2-yl)ethyl]thioureaHCID 3915018586%

반응 단계

{2-(1H-Benzimidazol-2-yl)ethylamine was made as the dihydrochloride salt according to a procedure described by Nicolaou et al. Bioorg. Med. Chem., 1998, 6, 1185-1208 and pretreated with DIPEA (2.07 mL, 11.86 mmol) for 5 minutes.} To a suspension of 2-(1H-benzimidazol-2-yl)ethylamine (1.39 g, 5.93 mmol) in dichloromethane (20 mL) was added benzoyl isothiocyanate (0.88 mL, 6.52 mmol). After 1 h, the reaction mixture was concentrated in vacuo. Ammonia in methanol (7N, 30 mL) was then added and the reaction stirred another 4 h. The excess ammonia and methanol were removed in vacuo and dichloromethane (15 mL) was added. The solid was removed by filtration and the filtrate concentrated in vacuo and purified by flash chromatography (methanol/dichloromethane, 5% then 10%) to give the title compound as a solid (1.12 g, 86% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026244B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-a74f91f5d9b844d1a4977d13d6fdf909
출처 메모uspto-grants-2011_09