Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672123Generated: November 1, 2026

Phosphorus oxychloride → 4-[(2-Fluoro-5-methyl-phenyl)amino]-6-(4-oxo-cyclohexyloxy)-7-methoxy-quinazoline

https://huagongshe.com/reaction/1672123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Fluoro-5-methylanilineHCID 262970—
Reactant4-Chloro-6-(1,4-dioxa-spiro[4,5]decan-8-yl-oxy)-7-methoxy-quinazolineHCID 59158225—
Reactant6-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-7-methoxy-3H-quinazolin-4-oneHCID 135991777—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product4-[(2-Fluoro-5-methyl-phenyl)amino]-6-(4-oxo-cyclohexyloxy)-7-methoxy-quinazolineHCID 58157253—

Reaction Conditions

Temperature40 °C

Reaction Steps

6 ml phosphorus oxychloride are added dropwise to 12.1 g 3,4-dihydro-4-oxo-6-(1,4-dioxa-spiro[4,5]decan-8-yl-oxy)-7-methoxy-quinazoline in 120 ml acetonitrile and the mixture is heated to an internal temperature of 40° C. Then 9.3 ml triethylamine are added dropwise and the reaction mixture is refluxed for 3 hours. The mixture is cooled to ambient temperature and after standing overnight half the solution of the intermediate product (4-chloro-6-(1,4-dioxa-spiro[4,5]decan-8-yl-oxy)-7-methoxy-quinazoline, see Example IX) is combined dropwise with 2.7 ml of 2-fluoro-5-methylaniline in 5 ml acetonitrile. The reaction mixture is heated to 40° C. for 3 hours, then cooled and evaporated down. The residue is mixed with water and stirred. The precipitate formed is suction filtered and divided between 1M sodium hydroxide solution and dichloromethane. The organic phase is separated off, dried, evaporated down and stirred with diisopropylether. The solid is suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998949B2
Source datasetuspto-grants-2011_08
ORD IDord-f58dfd88eb564c4db3a52f6672fd5dee
Source noteuspto-grants-2011_08