HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965348Generated: October 30, 2026
Trifluoroacetic acid → HCID 15522349, compound
https://huagongshe.com/reaction/965348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 22629250 | HCID 22629250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15522349 | HCID 15522349 | 62.4% |
Reaction Steps
To a solution of 3-[2-(2-t-butoxycarbonylmethyl-1-cycloheptenyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine (0.15 g) in dry dichloromethane (0.5 ml) at room temperature was added trifluoroacetic acid (0.46 ml). After stirring for one day at room temperature, the solution was partitioned between ethyl acetate and a saturated aqueous sodium bicarbonate. The separated aqueous layer was acidified with 1N-hydrochloric acid to pH 3 and extracted with ethyl acetate. The separated organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was recrystallized from ethanol--water to give 3-[2-(2-carboxymethyl-1-cycloheptenyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]- pyridine (0.083 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773530 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-06ceeb26b98f4bc7a4f7bd7fd1c20f55 |
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| Source note | uspto-grants-1998_06 |
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