Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346413Generated: October 23, 2026

4,5-Dichloro-2-fluoroaniline → 4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-nitroquinazoline

https://huagongshe.com/en/reaction/346413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5-Dichloro-2-fluoroanilineHCID 223091—
Reactant4-Chloro-6-nitroquinazolineHCID 11356257—
SolventIsopropanolHCID 3776—
Product4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-nitroquinazolineHCID 15480998—

Reaction Steps

3,4-Dichloro-6-fluoroaniline (1 equivalent, prepared as described in U.S. Pat. No. 6,126,917) was reacted with 4-chloro-6-nitroquinazoline (3.5 equivalents, prepared by reacting 6-nitroquinazoline with thionyl chloride, according to known procedures), in iso-propylalcohol. After filtration, 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-nitroquinazoline (compound 1) was obtained in 60% yield. m.p.=270–271° C.; MS (m/z): 353.2, 355.2 (M+); 1H-NMR: δ=6.97 (d, 1H), 7.345 (d, 1H), 7.885 (d, 1H), 8.405 (d, 1H), 8.554 (dd, 1H), 8.8 (d, 1H) ppm. HPLC conditions: C-18 column, 55% acetate buffer, PH=3.8/45% acetonitrile, flow=1 ml/min; r.t.=7.15 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07172749B2
Source datasetuspto-grants-2007_02
ORD IDord-83e5d3a1fcd541d29990cc006885a035
Source noteuspto-grants-2007_02