HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428863Generated: November 1, 2026
Potassium Hydroxide → HCID 136027596, compound
https://huagongshe.com/reaction/1428863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 136027629 | HCID 136027629 | — |
| Reactant | HCID 136337183 | HCID 136337183 | — |
| Reactant | HCID 136337184 | HCID 136337184 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136027596 | HCID 136027596 | — |
Reaction Steps
Aqueous 1M KOH (3.8 mL, 3.8 mmol) was added to a 3:2 mixture of 1-(7-dimethylamino-4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid ethyl ester and 1-(5-dimethylamino-4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (0.415 g, 1.27 mmol) in THF (3.8 mL). The reaction mixture was allowed to stir at room temperature for 18 h and was then concentrated. The residue was re-dissolved in water (10 mL) and acidified with 1M aqueous HCl (3 mL). The resulting precipitate was collected by filtration to yield a mixture of the titled compound and 1-(5-dimethylamino-4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid. The collected precipitate was triturated from DMSO and rinsed with ethanol to yield pure 1-(7-dimethylamino-4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid (0.113 mg, 29% yield). The filtrate was saved for further purification. MS (ESI/Cl): mass calcd. for C14H13N5O3, 299.1; m/z found, 300.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 12.97 (s, 1H), 12.21 (s, 1H), 8.92 (s, 1H), 8.22 (s, 1H), 7.90 (d, J=8.9 Hz, 1H), 6.93 (dd, J=9.0, 2.3 Hz, 1H), 6.72 (s, 1H), 3.07 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937078B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-62dc0efb60554ad793306c4d7509cd91 |
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| Source note | uspto-grants-2015_01 |
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