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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1521686생성일: 2026년 10월 27일

Methyl 2,2,2-trichloroacetimidate → Methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-(trichloromethyl)-1H-benzimidazole-6-carboxylate

https://huagongshe.com/reaction/1521686

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2,2,2-trichloroacetimidateHCID 100479—
반응물Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 11962077—
용매Acetic AcidHCID 176—
생성물Methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-(trichloromethyl)-1H-benzimidazole-6-carboxylateHCID 6723644580%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073926B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-9060c1155b03415da17abcf4f32591ef
출처 메모uspto-grants-2015_07