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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032793Generated: October 31, 2026

HCID 14851909, compound → HCID 14851920, compound

https://huagongshe.com/reaction/1032793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14851909HCID 14851909—
ReactantHCID 14894666HCID 14894666—
ProductHCID 14851920HCID 14851920—

Reaction Steps

The title compound was prepared by coupling 6-(2-fluorophenyl)-1-(trifluoromethyl)-8-iodo-4H-[1,2,4]triazolo [4,3-a][1,4]benzodiazepine with 3,4-dihydro-1-(2-propynyl)-2(1H)-quinolinone under the conditions used in Example 37. The product was purified by chromatoqraphy over the 50-fold amount of silica gel using 5% (v/v) of ethanol in methylene chloride. The clean fractions were combined and evaporated and the residue was crystallized from ethyl acetate to yield colorless crystals of 1-{3-[6-(2-fluorophenyl)-1-(trifluoromethyl)-4H-[1,2,4]triazolo[4,3-a][4,1]benzodiazepin-8-yl]-2-propynyl}-3,4-dihydro-2(1H)-quinolinone with m.p. 193°-196°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959361
Source datasetuspto-grants-1990_09
ORD IDord-576e9e54e20a4270b792c285e6e06fc6
Source noteuspto-grants-1990_09