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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698950Generated: October 27, 2026

7-Fluoro-6-nitroquinazolinone → 7-Fluoro-4-[(3-methylphenyl)-amino]-6-nitroquinazoline

https://huagongshe.com/reaction/1698950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Fluoro-6-nitroquinazolinoneHCID 18176168—
CatalystDimethylformamideHCID 6228—
SolventThionyl ChlorideHCID 24386—
Product7-Fluoro-4-[(3-methylphenyl)-amino]-6-nitroquinazolineHCID 10542070175.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

A suspension of 7-fluoro-6-nitroquinazolone (2.40 g, 11.48 mmol) in neat SOCl2 (25 mL) containing 2 drops of DMF was refluxed for 3 hours until it became clear. The excess SOCl2 was then removed in vacuo and dry benzene was added to the residue and then distilled under reduced pressure to remove all traces of SOCl2 giving crude 4-chloro-7-fluoro-6-nitroquinazoline, which was dissolved in dry CH2Cl2 (50 mL) and added to a stirred solution of m-toluidine in isopropanol (i-PrOH) (30 mL). The reaction mixture was stirred at 20° C. for 30 minutes and then hexane (200 mL) was added to precipitate the product as the HCl salt. The precipitate was filtered, washed with hexane, and then dissolved in MeOH/H2O (4:1, 150 mL) with gentle warming. Excess Et3N was then added to the solution followed by water (400 mL) to precipitate the product as the free base which was then filtered, washed with water and dried under reduced pressure to give 7-fluoro-4-[(3-methylphenyl)-amino]-6-nitroquinazoline (3.01 g, 88%) as a yellow powder, mp (CH2Cl2/hexane) 191-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344459B1
Source datasetuspto-grants-2002_02
ORD IDord-d014143cf7ff43d0b92366ea534682bb
Source noteuspto-grants-2002_02