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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232223Generated: November 1, 2026

Thionyl Chloride → HCID 21283340, compound

https://huagongshe.com/reaction/2232223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21283338HCID 21283338—
CatalystDimethylformamideHCID 6228—
SolventChloroformHCID 6212—
ProductHCID 21283340HCID 2128334085%

Reaction Steps

To 2.8 g of N-(3-hydroxypropyl)-N-methyl-3-(4-methoxy phenyl)-1,2,4-triazolo[3,4-a]phthalazin-6-amine (the compound of example 32) dissolved in chloroform (30 ml) are added a few drops of N,N-dimethylformamide and then 1.1 ml of thionyl chloride in chloroform (5 ml). The mixture is refluxed for about 5 hours. After cooling to room temperature, the mixture is concentrated to dryness and the residue is taken up with cold aqueous sodium bicarbonate. The product of the title is collected after filtration and crystallized from ethanol. Yield 85%. M.p. 113°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788186
Source datasetuspto-grants-1988_11
ORD IDord-d2e8a8714c7549b4b116a124db51c0ae
Source noteuspto-grants-1988_11