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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801877Generated: October 31, 2026

Sodium Bicarbonate → 4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(pyrrolidin-1-yliminomethyl)quinazoline

https://huagongshe.com/reaction/1801877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPyrrolidin-1-amine monohydrochlorideHCID 3017392—
Reactant4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino) 6-formylquinazolineHCID 57733656—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(pyrrolidin-1-yliminomethyl)quinazolineHCID 6875255381.4%

Reaction Steps

In a mixture of 1 mL of tetrahydrofuran and 0.1 mL of water were dissolved 40 mg of 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino) 6-formylquinazoline (IV-1) and 13 mg of 1-amino-pyrrolidine hydrochloride, followed by a reaction at room temperature overnight. After the reaction, aqueous saturated sodium bicarbonate solution was added, followed by extraction with ethyl acetate. The organic layer was dehydrated by passing through Presep (registered trademark), and the filtrate was concentrated. The concentrated residue was purified by chromatography (eluting with hexane:ethyl acetate-2:1→1:1) using an amino column to obtain 38 mg of 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(pyrrolidin-1-yliminomethyl)quinazoline (IX-1) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349857B2
Source datasetuspto-grants-2013_01
ORD IDord-ce1e43eb3af74c7e9c493e2c7bbbe257
Source noteuspto-grants-2013_01