HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240587Generated: October 31, 2026
Trifluoroacetic acid → 4-([1,2,4]Triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoic acid
https://huagongshe.com/reaction/240587
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoate | HCID 66937100 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-([1,2,4]Triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoic acid | HCID 66937264 | — |
Reaction Steps
A 25 ml flask was charged with tert-butyl 4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)-3-chloro-2-fluorobenzoate (0.060 g, 0.16 mmol) and dichloromethane (1.6 ml). The reaction was cooled to 0° C., and 2,2,2-trifluoroacetic acid (0.50 ml, 0.16 mmol) was added. The reaction was stirred for 20 minutes, then warmed to ambient temperature, stirred an additional 3 hours, and then concentrated to provide the desired product as a colorless oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648087B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-71a23a64da1143f1900d1e38a7096dce |
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| Source note | uspto-grants-2014_02 |
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