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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705508Generated: October 30, 2026

L-Tartaric acid → HCID 49856396, compound

https://huagongshe.com/reaction/705508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Tartaric acidHCID 444305—
Reactant6-(1H-Imidazol-1-yl)-2-phenylquinazolineHCID 24898732—
SolventNitromethaneHCID 6375—
ProductHCID 49856396HCID 49856396—

Reaction Conditions

Temperature60 °C

Reaction Steps

6-(1H-Imidazol-1-yl)-2-phenylquinazoline, 500 mg (1.8 mmol), is dissolved in 50 mL of nitromethane at reflux, with stirring and under a stream of nitrogen, 300 mg of L-tartaric acid are added, the mixture is stirred for a few minutes, it is filtered under nitrogen and the filtrate is heated to 60° C., evaporating off the solvent under a gentle vacuum, with stirring and under a stream of nitrogen, down to about ½ of the volume, and is then allowed to cool to 0° C. under nitrogen, stirred overnight at room temperature, and then filtered and dried at 30° C., 20 mmHg, for 24 hours. 520 mg of product are obtained in the form of yellow crystals, KF<0.5%, Calculated for C17H12N4.C4H6O6: C, 59.71; H, 4.30; N, 13.26. found: C, 59.76; H, 4.34; N, 13.22. XRPD form D. Form D heated at 40° C., 85% RH for 7 days gives an XRPD corresponding to form A, and an amorphous product when heated at 90° C. for 12 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174966B2
Source datasetuspto-grants-2015_11
ORD IDord-b0c15501b8924fa383520e424872ad92
Source noteuspto-grants-2015_11