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HRID 12630作成日:2026年10月26日

Ammonia → Benzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamate

https://huagongshe.com/reaction/12630

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物N-((Benzyloxy)carbonyl)-2-methylalanineHCID 294936—
反応物2,3-DiaminobenzamideHCID 10487029—
溶媒PyridineHCID 1049—
溶媒DimethylformamideHCID 6228—
生成物Benzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamateHCID 68512848—

反応条件

温度40 °C

反応手順

2-{[(Benzyloxy)carbonyl]amino}-2-methylpropanoic acid (5.18 g, 21.83 mmol) in a mixture of pyridine (25 mL) and DMF (25 mL) was treated with 1,1′-carbonyldiimidazole (3.72 g, 22.92 mmol) and heated at 40° C. for 2 hours. 2,3-Diaminobenzamide dihydrochlolide (4.89 g, 21.83 mmol), prepared as described in WO0026192, was added and the mixture was stirred at room temperature overnight. The solvents were removed under vacuum and the residue was partitioned between ethyl acetate and diluted sodium bicarbonate aqueous solution. The formed slightly yellow solid material was collected by filtration, washed with water and ethyl acetate, and dried to give Example 1A. MS (DCI/NH3) m/z 371 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728026B2
出典データセットuspto-grants-2010_06
ORD IDord-9c25fc59113f4ee5ad6fdc1b8bb23676
出典メモuspto-grants-2010_06