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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276938Generated: October 31, 2026

Trifluoroacetic acid → HCID 15522349, compound

https://huagongshe.com/reaction/276938

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 numberUS06355640B1
Source datasetuspto-grants-2002_03
ORD IDord-48a73ba58731427f9193cb7f09e32883
Source noteuspto-grants-2002_03