HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428864Generated: October 31, 2026
Potassium Hydroxide → HCID 136027629, compound
https://huagongshe.com/reaction/1428864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 136027596 | HCID 136027596 | — |
| Reactant | HCID 136337183 | HCID 136337183 | — |
| Reactant | HCID 136337184 | HCID 136337184 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136027629 | HCID 136027629 | — |
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 aqueous HCl (1 M, 3 mL). The resulting precipitate was collected by filtration to yield a mixture of the titled compound and 1-(7-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. The filtrate from the trituration was purified by reverse-phase HPLC to yield the titled compound (49.7 mg, 13% yield). MS (ESI/Cl): mass calcd. for C14H13N5O3, 299.1; m/z found, 300.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 12.99 (s, 2H), 8.96 (d, J=0.6 Hz, 1H), 8.25 (s, 1H), 7.84 (t, J=8.1 Hz, 1H), 7.67-7.48 (m, 2H), 3.12 (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-b262f43ed0524437a5995ac0fd8e0def |
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| Source note | uspto-grants-2015_01 |
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