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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215922Generated: October 29, 2026

2-(1H-pyrrol-1-yl)benzaldehyde → N4-(1-(2-(1H-Pyrrol-1-yl)benzyl)piperidin-4-yl)-N2-(3-(dimethylamino)propyl)quinazoline-2,4-diamine

https://huagongshe.com/reaction/215922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1H-pyrrol-1-yl)benzaldehydeHCID 4961259—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN2-(3-(Dimethylamino)propyl)-N4-(piperidin-4-yl)quinazoline-2,4-diamineHCID 58006203—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductN4-(1-(2-(1H-Pyrrol-1-yl)benzyl)piperidin-4-yl)-N2-(3-(dimethylamino)propyl)quinazoline-2,4-diamineHCID 58006247—

Reaction Steps

N2-(3-(Dimethylamino)propyl)-N4-(piperidin-4-yl)quinazoline-2,4-diamine (62 mg, 0.189 mmol), 2-(1H-pyrrol-1-yl)benzaldehyde (32 mg, 0.189 mmol), NaCNBH3 (12 mg, 0.190 mmol) and ZnCl2 (13 mg, 0.09 mmol) in MeOH (1 ml) was stirred at room temperature overnight. The solvent was removed under reduced pressure, and 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-5378b0a46d514d1dad5b383f27eb4f9c
Source noteuspto-grants-2012_06