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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284644Generated: October 30, 2026

M-Phenylenediamine → HCID 90052375, compound

https://huagongshe.com/reaction/2284644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-PhenylenediamineHCID 7935—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
ReactantSodium BicarbonateHCID 516892—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 90052375HCID 9005237566.2%

Reaction Steps

To a solution of N-Boc-β-alanine (1.00 g) in N,N-dimethylactamide (5 mL), carbonyldiimidazole (888 mg) was added at room temperature, and the mixture was stirred at the same temperature for 1 hour and 20 minutes. To the reaction mixture, a solution of 1,3-phenylenediamine (1.15 g) in N,N-dimethylactamide (5 mL) was added at room temperature, and the mixture was stirred at the same temperature for 18 hours. To the reaction mixture, saturated aqueous sodium hydrogencarbonate and ethyl acetate were added. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain tert-butyl (3-((3-aminophenyl)amino)-3-oxopropyl)carbamate (B6, 978 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-61a7e208ba59411d8b6b46ef8b8b1523
Source noteuspto-grants-2015_09