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HRID 2081014作成日:2026年10月25日

Ethylmorpholine → HCID 25094622、化合物

https://huagongshe.com/reaction/2081014

反応式

関与物質

役割名称HCID仕込み量
反応物EthylmorpholineHCID 7525—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物2-Chloro-3-(trifluoromethyl)benzylamineHCID 5224207—
反応物3-methyl-1-(1-methyl-1H-imidazol-2-yl)-2-oxo-4-imidazolidinecarboxylic acidHCID 67103405—
溶媒DichloromethaneHCID 6344—
生成物HCID 25094622HCID 2509462231.2%

反応手順

A solution of 3-methyl-1-(1-methyl-1H-imidazol-2-yl)-2-oxo-4-imidazolidinecarboxylic acid (166 mg, 0.517 mmol) and N-ethyl morpholine (0.397 ml, 3.10 mmol) in dichloromethane (5 ml) was treated with 1-hydroxybenzotriazole hydrate (95 mg, 0.620 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (99 mg, 0.517 mmol) and stirred at room temperature for 10 minutes. 1-[2-Chloro-3-(trifluoromethyl)phenyl]methanamine (108 mg, 0.517 mmol) was then added and the reaction stirred overnight at room temperature. The reaction mixture was diluted with dichloromethane and washed with saturated sodium hydrogen carbonate solution, water and brine, separated through a hydrophobic frit and the organic layer was reduced under vacuum. The residue was purified by mass-directed automated HPLC to give N-{[2-chloro-3-(trifluoromethyl)phenyl]methyl}-3-methyl-1-(1-methyl-1H-imidazol-2-yl)-2-oxo-4-imidazolidinecarboxamide (67 mg, 29.6% yield). LC/MS [M+H]+=416, retention time=1.89 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07932282B2
出典データセットuspto-grants-2011_04
ORD IDord-2890629326584f5f8492786531889469
出典メモuspto-grants-2011_04