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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443828Generated: October 30, 2026

HCID 178513504, compound → HCID 178513502, compound

https://huagongshe.com/reaction/443828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178513504HCID 178513504—
ReactantHCID 178524062HCID 178524062—
CatalystPyridineHCID 1049—
SolventThionyl ChlorideHCID 24386—
ProductHCID 178513502HCID 178513502—

Reaction Steps

A mixture of 4,9-dihydro-9-oxo-pyrazolo[5,1-b]-quinazoline-2-carboxylic acid (5 g; 0.022 mole), thionyl chloride (250 ml) and four drops of pyridine is stirred at room temperature for 24 hrs. The reaction mixture is evaporated to dryness under reduced pressure in a water bath at 30°-40° C. The residue is treated with cold (0° C.) concentrated ammonium hydroxide solution (200 ml) and allowed to come to room temperature. The product is filtered off, washed with ether and used in the next step without further purification. Yield 3.2 g; mp 315°-325° C. An analytical sample, recrystallized from dimethylformamide, melts at 335°-340° C. By the same procedure, starting with the corresponding 7-fluoro compound, the product obtained is 4,9-dihydro-7-fluoro-9-oxo-pyrazolo[5,1-b]quinazoline-2-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261996
Source datasetuspto-grants-1981_04
ORD IDord-2d0d3e7f568a4483a1c31019a7c68c7a
Source noteuspto-grants-1981_04