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HRID 1170693作成日:2026年10月25日

Hydrochloric Acid → 2-[2-(3-Chloro-benzyl)-5,6-difluoro-benzoimidazol-1-yl]-2,N-dicyclohexyl-acetamide

https://huagongshe.com/reaction/1170693

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物3-Chlorophenylacetic acidHCID 15879—
反応物CyclohexanecarboxaldehydeHCID 16275—
反応物Cyclohexyl isocyanideHCID 79129—
反応物tert-Butyl (2-amino-4,5-difluorophenyl)carbamateHCID 66619231—
溶媒MethanolHCID 887—
溶媒1,4-DioxaneHCID 31275—
生成物2-[2-(3-Chloro-benzyl)-5,6-difluoro-benzoimidazol-1-yl]-2,N-dicyclohexyl-acetamideHCID 6737214121%

反応手順

To a solution of (2-amino-4,5-difluoro-phenyl)-carbamic acid tert-butyl ester (36.64 mg, 0.15 mmol, 1.0 equiv) in methanol (2.0 mL) was added cyclohexanecarbaldehyde (25.80 mg, 27.08 μL, 0.23 mmol, 1.5 equiv; [2043-61-0]) and the mixture stirred at rt. After 30 min, (3-chloro-phenyl)-acetic acid (34.12 mg, 0.20 mmol, 1.33 equiv; [CAS RN 1878-65-5]) and cyclohexyl isocyanide (16.38 mg, 18.41 μL, 0.15 mmol, 1.0 equiv; [931-53-3]) were added and stirring continued at rt for 2 h. A solution of 4 M HCl in dioxane (0.2 mL) was added and the reaction mixture stirred at rt overnight. Removal of the solvent mixture under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 15.7 mg (21%) of the title compound. MS (ISP): 500.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07825258B2
出典データセットuspto-grants-2010_11
ORD IDord-64af66e21b8a46c6a3982d0a2022a8e1
出典メモuspto-grants-2010_11