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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428863Generated: November 1, 2026

Potassium Hydroxide → HCID 136027596, compound

https://huagongshe.com/reaction/1428863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 136027629HCID 136027629—
ReactantHCID 136337183HCID 136337183—
ReactantHCID 136337184HCID 136337184—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136027596HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937078B2
Source datasetuspto-grants-2015_01
ORD IDord-62dc0efb60554ad793306c4d7509cd91
Source noteuspto-grants-2015_01