HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645362Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 24771610, compound
https://huagongshe.com/reaction/645362
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 68616693 | HCID 68616693 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 24771610 | HCID 24771610 | 65.6% |
Reaction Steps
A solution of 110 mg of N-(4-fluorophenyl)-6-(1-hydroxy-1-methylethyl)imidazo[1,2-a]pyridine-2-carboxamide and 3.3 mg of para-toluenesulfonic acid in 5 ml of xylene is heated at reflux for 6 hours and then evaporated to dryness under reduced pressure. The residue is taken up in 200 ml of dichloromethane and 20 ml of water. The organic phase is dried and concentrated, and the residue is purified by chromatography on silica, elution being carried out with a mixture of dichloromethane and ethyl acetate (95/5). The fractions comprising the expected product are combined and concentrated to dryness. The residue is triturated and washed with ethyl ether, filtered off and dried to give 68 mg of N-(4-fluorophenyl)-6-isopropenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07704989B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-70dfa5adbdef45c086482b50b1cdea3d |
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| Source note | uspto-grants-2010_04 |
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