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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428864Generated: October 31, 2026

Potassium Hydroxide → HCID 136027629, compound

https://huagongshe.com/reaction/1428864

Reaction equation

Participants

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937078B2
Source datasetuspto-grants-2015_01
ORD IDord-b262f43ed0524437a5995ac0fd8e0def
Source noteuspto-grants-2015_01