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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336774Generated: October 30, 2026

3,5-Dimethylbenzoyl Chloride → HCID 135907961, compound

https://huagongshe.com/reaction/336774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethylbenzoyl ChlorideHCID 81088—
Reactant2-Amino-4,6-dimethoxybenzamideHCID 20349016—
SolventTetrahydrofuranHCID 8028—
ProductHCID 135907961HCID 135907961—

Reaction Steps

A mixture of 2-amino-4,6-dimethoxybenzamide (0.0700 g, 0.36 mmol) and 3,5-dimethylbenzoyl chloride (0.112 g, 0.65 mmol) in THF (5.0 mL) was placed in a microwave reactor at 80° C. for 30 min. The THF was removed under reduced pressure, and the residue was purified via CombiFlash chromatography to yield the expected amide. This material was used directly in the next step. A mixture of the amide and H2O/MeCN (2:1, 5.00 mL) was basified to pH 12 with 2 N NaOH and stirred at 80° C. for 16 h. The mixture was cooled and neutralized with 1 N HCl. The resulting precipitate was collected on a frit, washed with water (5.00 mL) and lyophilized to yield 2-(3,5-dimethylphenyl)-5,7-dimethoxyquinazolin-4(3H)-one (0.0395 g, 31% over two steps) as a white solid. Selected data: 1H NMR (300 MHz, DMSO-d6) δ 11.88 (s, 1H), 7.80 (s, 2H), 7.21 (s, 1H), 6.76 (d, J=2.24 Hz, 1H), 6.53 (d, J=2.21 Hz, 1H), 3.89 (s, 3H), 3.85 (s, 3H), 2.35 (s, 6H); MS (APCI) m/z 311 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889698B2
Source datasetuspto-grants-2014_11
ORD IDord-60259de18f774905a6fdd7d1be21d160
Source noteuspto-grants-2014_11