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HRID 1521686作成日:2026年10月27日

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

https://huagongshe.com/reaction/1521686

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2,2,2-trichloroacetimidateHCID 100479—
反応物Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 11962077—
溶媒Acetic AcidHCID 176—
生成物Methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-(trichloromethyl)-1H-benzimidazole-6-carboxylateHCID 6723644580%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073926B2
出典データセットuspto-grants-2015_07
ORD IDord-9060c1155b03415da17abcf4f32591ef
出典メモuspto-grants-2015_07