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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402523Generated: November 2, 2026

4-Aminobenzoic Acid → HCID 57663055, compound

https://huagongshe.com/reaction/2402523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178517434HCID 178517434—
Solvent1-ButanolHCID 263—
ProductHCID 57663055HCID 5766305548.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 4-cyclohexylquinazolin-2(1H)-one (500 mg, 2.2 mmol) and phosphorous oxychloride (10 mL, 111 mmol) was heated to reflux for 1 h. The volatiles were removed under reduced pressure, and then the residue was treated with ice water and extracted with ethyl acetate. The combined organic extracts were washed with saturated sodium chloride and dried over sodium sulfate. The solvent was removed on a rotary evaporator, and to this residue was added 4-aminobenzoic acid (300 mg, 2.2 mmol), triethylamine (435 μL, 3.0 mmol) and n-butanol (5 mL). This mixture was heated to 140° C. for 25 min. The mixture was cooled to rt and triturated with ether. The residual solid was collected via vacuum filtration, washed with ether and dried to afford 4-(4-cyclohexylquinazolin-2-ylamino)benzoic acid (370 mg, 48%) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796294B2
Source datasetuspto-grants-2014_08
ORD IDord-f37e24c9e5ed44778b6cbc2c1bd09793
Source noteuspto-grants-2014_08