HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405783Generated: October 30, 2026
Hydrochloric Acid → 7-(Trifluoromethyl)imidazo[1,2-a]pyridine-3-carboxylic acid
https://huagongshe.com/reaction/405783
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86677442 | HCID 86677442 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 7-(Trifluoromethyl)imidazo[1,2-a]pyridine-3-carboxylic acid | HCID 71280482 | — |
Reaction Steps
To a stirring solution of ethyl 7-(trifluoromethyl)imidazo[1,2-a]pyridine-3-carboxylate (23) (100 mg, 0.387 mmol) in THF:MeOH (4:1, 1.5 mL) was added 2N LiOH (0.25 mL). The reaction was heated at 60° C. for 1 hour. Then, cooled to room temperature and the pH was adjusted between 4-5 with 1N HCl. The solvent was partially concentrated and the resulting aqueous layer was lyophilized to give 7-(trifluoromethyl)imidazo[1,2-a]pyridine-3-carboxylic acid (24). 1H NMR (400 MHz, d6-DMSO) δ 9.44 (d, J=7.2 Hz, 1H), 8.40 (s, 1H), 8.31-8.30 (m, 1H), 7.48 (dd, J=2.0, 7.6 Hz, 1H). MS m/z 231.2 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754071B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f784496733094d62bc1c3696b175fd6b |
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| Source note | uspto-grants-2014_06 |
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