HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443828Generated: October 30, 2026
HCID 178513504, compound → HCID 178513502, compound
https://huagongshe.com/reaction/443828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178513504 | HCID 178513504 | — |
| Reactant | HCID 178524062 | HCID 178524062 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 178513502 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261996 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-2d0d3e7f568a4483a1c31019a7c68c7a |
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| Source note | uspto-grants-1981_04 |
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