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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412000Generated: October 29, 2026

HCID 18535765, compound → HCID 18535766, compound

https://huagongshe.com/reaction/412000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18535765HCID 18535765—
CatalystNickelHCID 935—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 18535766HCID 1853576683.3%

Reaction Steps

A solution of 6-amino-4-(4-benzyloxyanilino)quinazoline hydrochloride (1.46 g, 3.57 mmol) in methanol/THF (1:1, 100 mL) was hydrogenated over Raney nickel (1 g) at 51.5 psi and 23° C. for 18 hours. The reaction mixture was celite filtered, and the volatiles were removed under reduced pressure. The crystalline brown 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), dried in a vacuum oven at 60° C., and then purified by flash chromatography on silica gel, eluting with CHCl3 then 4% MeOH in CHCl3 to give 6-amino-4-(4-benzyloxyanilino)quinazoline (1.018 g, 80%) as a cream powder; mp 173-175° C., remelt 240-245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562818B1
Source datasetuspto-grants-2003_05
ORD IDord-b0f8d0fe20f04d568eaf507e5131253a
Source noteuspto-grants-2003_05