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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406821Generated: October 30, 2026

Cyclopropylamine → N-{5-[(cyclopropylamino)methyl]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

https://huagongshe.com/reaction/406821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(5-formyl-2-methylphenyl)-4-[(4-phenylquinazolin-2-yl)amino]benzamideHCID 57662899—
CatalystAcetic AcidHCID 176—
CatalystTetrahydrofuranHCID 8028—
SolventDichloromethaneHCID 6344—
ProductN-{5-[(cyclopropylamino)methyl]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamideHCID 5766297552.4%

Reaction Steps

A mixture of N-(5-formyl-2-methylphenyl)-4-(4-phenylquinazolin-2-ylamino)benzamide (250 mg, 0.546 mmol), cyclopropylamine (238 μL, 3.44 mmol), dichloromethane (10 m:), tetrahydrofuran (2 drops) and acetic acid (2 drops) was stirred at rt for 1 h. Sodium triacetoxyborohydride (275 mg, 1.30 mmol) was added and the mixture was stirred overnight. The crude reaction was diluted with dichloromethane, washed with saturated sodium bicarbonate and saturated sodium chloride and dried over sodium sulfate. The solution was concentrated on a rotary evaporator and purified by HPLC to give a yellow solid (143 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754092B2
Source datasetuspto-grants-2014_06
ORD IDord-f749afbdbd85452f8219f9a73565c082
Source noteuspto-grants-2014_06