참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzoyl isothiocyanate | HCID 68284 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| 반응물 | 2-(1H-Benzimidazol-2-yl)ethan-1-amine | HCID 415158 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-[2-(1H-Benzimidazol-2-yl)ethyl]thiourea | HCID 39150185 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08026244B2 |
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| 출처 데이터셋 | uspto-grants-2011_09 |
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| ORD ID | ord-a74f91f5d9b844d1a4977d13d6fdf909 |
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| 출처 메모 | uspto-grants-2011_09 |
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