Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl 2,2,2-trichloroacetimidate → Methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-(trichloromethyl)-1H-benzimidazole-6-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl 2,2,2-trichloroacetimidate | HCID 100479 | — |
| 반응물 | Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate | HCID 11962077 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | Methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-(trichloromethyl)-1H-benzimidazole-6-carboxylate | HCID 67236445 | 80% |
반응 단계
To a stirred solution of methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate (4.7 g, 14.5 mmol) in acetic acid (50 mL) is added methyl trichloroacetimidate (3.1 g, 17.4 mmol). After 3 h at room temperature, the solvent is evaporated, the residue is dissolved in EtOAc, and is washed with Na2CO3 and brine. The organic layer is dried (Na2SO4) and evaporated. The residue is triturated with hexanes to afford the title compound (5.2 g, 80%) as a fine powder. LCMS (Method T), 1.85 min, 450.63 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09073926B2 |
| 출처 데이터셋 | uspto-grants-2015_07 |
| ORD ID | ord-9060c1155b03415da17abcf4f32591ef |
| 출처 메모 | uspto-grants-2015_07 |