HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515212Generated: October 30, 2026
4-Aminobenzoic Acid → HCID 57663055, compound
https://huagongshe.com/reaction/1515212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178517434 | HCID 178517434 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 57663055 | HCID 57663055 | 48.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222263B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-a90648d3594f4f1ab424ffcaa5e2c6a5 |
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| Source note | uspto-grants-2012_07 |
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