Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264051Generated: October 26, 2026

1,1-Dichloroethane → (6-Iodoquinazolin-4-yl)-(3-methyl-4-phenoxy-phenyl)-amine

https://huagongshe.com/reaction/1264051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
Reactant4-Chloro-6-iodoquinazolineHCID 11173809—
Reactant3-Methyl-4-phenoxyanilineHCID 15550488—
Solventtert-ButanolHCID 6386—
Product(6-Iodoquinazolin-4-yl)-(3-methyl-4-phenoxy-phenyl)-amineHCID 18616443—

Reaction Conditions

Temperature90 °C

Reaction Steps

The 4-chloro-6-iodo-quinazoline (5.0 g, 17.2 mmol) and the 3-methyl-4-phenoxyaniline (17.2 mmol) were mixed together in 1:1 dichloroethane and t-butanol (50 ml). The reaction mixture was heated at 90° C. for 4 hours whereupon a yellow precipitate was observed. The reaction was cooled down and the precipitate was collected and afforded (6-iodo-quinazolin-4-yl)-(3-methyl-4-phenoxy-phenyl)-amine. (8.0 g, 94%). M/z, 454. 1H NMR (CD3OD): δ: 9.12(s, 1H), 8.83(s, 1H), 8.39 (d, 1H, J=8.8 Hz), 7.63(d, 1H, J=8.8 Hz), 7.55 (d, 1H, J=2.1 Hz), 7.35(dd,1H, J1=J2=8.5 Hz), 7.28(t, 2H, J=8.1 Hz, ), 7.05 (t, J=8.5 Hz), 6.87(d, 1H, J=8.1 Hz), 3.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541481B2
Source datasetuspto-grants-2003_04
ORD IDord-f1214ae0559e4d23b162c482b4aefd50
Source noteuspto-grants-2003_04