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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032781Generated: November 2, 2026

Ethanol → HCID 12434322, compound

https://huagongshe.com/reaction/1032781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-(2-chlorophenyl)-2-iodo-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepineHCID 14851924—
Reactant7‐Fluoro‐4‐(prop‐2‐yn‐1‐yl)‐3,4‐dihydro‐2H‐1,4‐ benzoxazin‐3‐oneHCID 14851959—
SolventDichloromethaneHCID 6344—
ProductHCID 12434322HCID 12434322—

Reaction Steps

The title compound was prepared by reacting 4-(2-chlorophenyl)-2-iodo-9-methyl-6H-thieno-[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine with 7-fluoro-4-(2-propynyl)-2H-1,4-benzoxazin-3(4H)-one under the conditions used in Example 37. The product was isolated by chromatography over the 50 fold amount of silica gel using 4 % (v/v) of ethanol in methylene chloride. The good fractions were combined and evaporated and the residue was crystallized from ethyl acetate to give colorless crystals of 4-{3-[4-(2-chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin.2.2-propynyl}-7-fluoro-2H-1,4-benzoxazin-3(4H)-one with m.p. 215°-217°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959361
Source datasetuspto-grants-1990_09
ORD IDord-1174a79f33034eef98c9e2f2f6472969
Source noteuspto-grants-1990_09