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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215923Generated: October 30, 2026

Sodium cyanoborohydride → N4-(1-(2-(1H-Imidazol-1-yl)benzyl)piperidin-4-yl)-N2-(3-(diethylamino)propyl)quinazoline-2,4-diamine

https://huagongshe.com/reaction/215923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(1H-imidazol-1-yl)benzaldehydeHCID 10419625—
ReactantN2-(3-(Dimethylamino)propyl)-N4-(piperidin-4-yl)quinazoline-2,4-diamineHCID 58006203—
ReactantN2-(3-(diethylamino)propyl)-N4-(piperidin-4-yl)quinazoline-2,4-diamineHCID 67027548—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductN4-(1-(2-(1H-Imidazol-1-yl)benzyl)piperidin-4-yl)-N2-(3-(diethylamino)propyl)quinazoline-2,4-diamineHCID 58006232—

Reaction Steps

To a solution of 57 mg (0.160 mmol) N2-(3-(diethylamino)propyl)-N4-(piperidin-4-yl)quinazoline-2,4-diamine (prepared analogously to Compound 129) and 2-(1H-imidazol-1-yl)benzaldehyde (28 mg, 0.160 mmol) in MeOH (1 ml) was added NaCNBH3 (10 mg, 0.160 mmol) and ZnCl2 (11 mg, 0.08 mmol), The solution was stirred at room temperature overnight. Solvent was removed under reduced pressure. The crude product was purified by silica gel chromatography using 5% NH3 ca. 7 N MeOH in CH2Cl2 and 90% CH2Cl2 solution as eluent to produce the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193203B2
Source datasetuspto-grants-2012_06
ORD IDord-6800b49fd2fd48acb30e628063aa796a
Source noteuspto-grants-2012_06