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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965348Generated: October 30, 2026

Trifluoroacetic acid → HCID 15522349, compound

https://huagongshe.com/reaction/965348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22629250HCID 22629250—
SolventDichloromethaneHCID 6344—
ProductHCID 15522349HCID 1552234962.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773530
Source datasetuspto-grants-1998_06
ORD IDord-06ceeb26b98f4bc7a4f7bd7fd1c20f55
Source noteuspto-grants-1998_06