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HRID 1293088作成日:2026年10月26日

Potassium Sodium Tartrate → 2-chloro-N-(cyclopropylmethyl)-1-mesityl-N-propyl-6-(trifluoromethyl)-1H-imidazo[1,2-a]imidazole-5-carboxamide

https://huagongshe.com/reaction/1293088

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Sodium TartrateHCID 9357—
反応物Cyclopropanemethanamine, N-propyl-HCID 117787—
反応物TrimethylaluminumHCID 16682925—
反応物6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[1,2-a]imidazole-3-carboxylic Acid Ethyl EsterHCID 20780223—
溶媒TolueneHCID 1140—
生成物2-chloro-N-(cyclopropylmethyl)-1-mesityl-N-propyl-6-(trifluoromethyl)-1H-imidazo[1,2-a]imidazole-5-carboxamideHCID 20780009—

反応手順

To a solution of N-cyclopropylmethylpropylamine (0.22 mL, 1.530 mmol) in toluene (1.5 mL) at 0° C. was added 2.0M solution of trimethylaluminum in toluene (0.77 mL, 1.530 mmol). The clear solution was warmed to room temperature and stirred for 1 h. A solution of 6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[1,2-a]imidazole-3-carboxylic acid ethyl ester (37.7 mg, 0.094 mmol) in toluene (1.0 mL) was added at 0° C. via cannula. The reaction mixture was heated at 80° C. for 2 h. A solution of Rochelle's salt (2.0 mL) was added carefully at 0° C. and the mixture was vigorously stirred for 30 min. The crude product was extracted with ethyl acetate. The combined organic extracts were dried with MgSO4. The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase preparative HPLC. Yield—39.5 mg (90%). LC/MS: tR=1.93 min., MS: [M+H]=467.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07238699B2
出典データセットuspto-grants-2007_07
ORD IDord-d25d13ec0289413b8fa2c5b7481787e0
出典メモuspto-grants-2007_07