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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406824Generated: October 25, 2026

Water → Methyl 3-methyl-4-(4-phenylquinazolin-2-ylamino)benzoate

https://huagongshe.com/reaction/406824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl 4-amino-3-methylbenzoateHCID 2736799—
Reactant2-Chloro-4-phenylquinazolineHCID 3123582—
Solvent1-ButanolHCID 263—
ProductMethyl 3-methyl-4-(4-phenylquinazolin-2-ylamino)benzoateHCID 6893037679.6%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 2-chloro-4-phenylquinazoline (200 mg, 0.83 mmol) and methyl 4-amino-3-methylbenzoate (137 mg, 0.83 mmol) in n-butanol was heated to 160° C. for 1 h and then cooled to rt. Water (10 mL) was added and the product collected by filtration to give the methyl 3-methyl-4-(4-phenylquinazolin-2-ylamino)benzoate (244 mg, 79%), which was dissolved in a 1:1 mixture of water and methanol (10 mL) containing sodium hydroxide (100 mg, 2.5 mmol). The mixture was heated to 60° C. overnight. Ethyl acetate (100 mL) was added and the phases were separated. The aqueous layer was acidified with 10% aqueous hydrochloric acid and extracted with ethyl acetate. The organic extracts were dried over sodium sulfate, filtered and concentrated on a rotary evaporator to give 3-methyl-4-(4-phenylquinazolin-2-ylamino)benzoic acid (188 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754092B2
Source datasetuspto-grants-2014_06
ORD IDord-b8de520c226d48c6a33e942a8d803f2d
Source noteuspto-grants-2014_06