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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379036Generated: October 30, 2026

Pyridine → HCID 70110849, compound

https://huagongshe.com/reaction/1379036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantHCID 135554955HCID 135554955—
SolventWaterHCID 962—
ProductHCID 70110849HCID 7011084972.3%

Reaction Conditions

Temperature4 °C

Reaction Steps

To a mixture of 7-(4-fluorophenyl)-8-(pyridin-4-yl)-1,2,3,4-tetrahydropyrazolo[5,1-c][1,2,4]triazine (118 mg) and pyridine (64 mg) in N-methyl-1-pyrrolidone (2 ml) was added phenylacetyl chloride (65 mg) under nitrogen atmosphere with ice cooling. After stirring for 1 hour at 4° C., the reaction mixture was poured into cold water. The separated oil was extracted with ethyl acetate and the extract was washed with brine, dried and concentrated in vacuo. The residue was purified by column chromatography on silica gel and the obtain oil was dissolved in 10% methanolic hydrogen chloride (1 ml). The resulting clear solution was concentrated in vacuo. The residue was crystallized from ethyl acetate to give 7-(4-fluorophenyl)-2-phenylacetyl-8-(pyridin-4-yl)-1,2,3,4-tetrahydropyrazolo[5,1-c][1,2,4]triazine hydrochloride (130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670503
Source datasetuspto-grants-1997_09
ORD IDord-832b3cc3273b49f9890a43b149c3f6f1
Source noteuspto-grants-1997_09