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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411996Generated: October 29, 2026

HCID 18535967, compound → HCID 11659911, compound

https://huagongshe.com/reaction/411996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18535967HCID 18535967—
CatalystNickelHCID 935—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 11659911HCID 1165991180.7%

Reaction Steps

A solution of 6-amino-4-(4-phenoxyanilino)quinazoline hydrochloride (1.65 g, 4.2 mmol) in methanol/THF (1:1, 100 mL) was hydrogenated over Raney nickel (1 g) at 50 psi and 27° C. for 18 hours. The reaction mixture was celite filtered, and the volatiles were removed under reduced pressure. The glassy residue was partially redissolved in MeOH (25 mL), and dilute aqueous Na2CO3 solution (0.1 M, 50 mL) was added with vigourous stirring. After 2 hours, the precipitate was collected by Buchner filtration, rinsed with water (50 mL), air dried, and then purified by flash chromatography on silica gel, eluting with 2.5% then 4% MeOH in CH2Cl2 to give 6-amino-4-(4-phenoxyanilino)quinazoline (1.113 g, 80%) as a pale yellow glassy foam;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562818B1
Source datasetuspto-grants-2003_05
ORD IDord-d3860102d3d040c7a9f84a031a53ddfe
Source noteuspto-grants-2003_05