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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12630Generated: October 26, 2026

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

https://huagongshe.com/reaction/12630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-((Benzyloxy)carbonyl)-2-methylalanineHCID 294936—
Reactant2,3-DiaminobenzamideHCID 10487029—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductBenzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamateHCID 68512848—

Reaction Conditions

Temperature40 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728026B2
Source datasetuspto-grants-2010_06
ORD IDord-9c25fc59113f4ee5ad6fdc1b8bb23676
Source noteuspto-grants-2010_06