HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219086Generated: October 29, 2026
4-Aminobenzoic Acid → HCID 18510721, compound
https://huagongshe.com/reaction/2219086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18510746 | HCID 18510746 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18510721 | HCID 18510721 | 36.9% |
Reaction Steps
A solution of 4-aminobenzoic acid (0.020 mol) and N-ethyl-N-(1-methylethyl)-2-propanamine, (0.020 mol) in CH2Cl2 (100 ml) was cooled to 0° C. (±)-4,5-dihydro-3-(3-pyridinyl)-5-isoxazolecarbonyl chloride monohydrochloride (0.020 mol) was added. The resulting brown suspension was stirred overnight. The precipitate was filtered off, washed with CH2Cl2, then dried. The filtrate was evaporated under reduced pressure. The residue was purified by short column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5). The pure fractions were collected and the solvent was evaporated under reduced pressure. The residue was stirred in methanol, filtered off, then dried, yielding 2.3 g of (±)-4-[[[4,5-dihydro-3-(3-pyridinyl)-5-isoxazolyl]-carbonyl]amino]benzoic acid (interm. 19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414048B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-dffc631e7abc4431a665fe7454193103 |
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| Source note | uspto-grants-2008_08 |
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