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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515212Generated: October 30, 2026

4-Aminobenzoic Acid → HCID 57663055, compound

https://huagongshe.com/reaction/1515212

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 numberUS08222263B2
Source datasetuspto-grants-2012_07
ORD IDord-a90648d3594f4f1ab424ffcaa5e2c6a5
Source noteuspto-grants-2012_07