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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220116Generated: October 28, 2026

Sodium Hydroxide → HCID 86630921, compound

https://huagongshe.com/reaction/220116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86630919HCID 86630919—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86630921HCID 8663092134.9%

Reaction Steps

In 2.6 ml of a mixture (1:1) of tetrahydrofuran and methanol was dissolved 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(4 (N-(2-(methanesulfonyl)ethyl)-2,2,2-trifluoroacetamido)butyloxyimino)quinazoline (V-14, 40 mg), and 86 μl of 1 mol/L aqueous sodium hydroxide solution was added, followed by stirring at room temperature for 14 hours, and at 40° C. for 2 hour. After the reaction, the reaction mixture was extracted with ethyl acetate, the organic layer was dried, and filtrate was concentrated. The concentrated residue was purified by chromatography (eluting with 0 to 3% methanol-contenting ethyl acetated) using an amino column, and the resulting pale yellow oil was powdered with a mixture of hexane and ethyl acetate to obtain 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(4-(2-(methanesulfonyl)ethylamino)butyloxyimino)quinazoline (V-15, 12 mg) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202879B2
Source datasetuspto-grants-2012_06
ORD IDord-c7e209332e494813b15ce12297b9569e
Source noteuspto-grants-2012_06