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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237603Generated: November 2, 2026

P-Anisidine → HCID 178492352, compound

https://huagongshe.com/reaction/2237603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178423396HCID 178423396—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178492352HCID 17849235285.4%

Reaction Steps

To a solution of 2.04 g of 4-{[(1S,2R)-2-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)cyclohexyl]amino}-6-methylquinazoline-2-carboxylic acid, 694 mg of 4-methoxyaniline, 1.08 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 762 mg of 1-hydroxybenzotriazole in 40 ml of N,N′-dimethylformamide, 1.57 ml of triethylamine was added, and then the mixture was stirred at room temperature for 24 hours. The reaction solution was mixed with water and then extracted with ethyl acetate. The organic layer was washed with water and saturated brine and then dried over magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (chloroform) to obtain 2.08 g of the desirable compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718663B2
Source datasetuspto-grants-2010_05
ORD IDord-0ccd8c175f7345deae4a1ca4e31921b3
Source noteuspto-grants-2010_05