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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698938Generated: October 26, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → 3-[4-(3-Bromo-phenylamino)-quinazolin-7-ylcarbamoyl]acrylic acid ethyl ester

https://huagongshe.com/reaction/1698938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant7-Amino-4-[(3-bromophenyl)amino]quinazolineHCID 5328045—
Reactant2-Butenedioic acid, monoethyl esterHCID 5878225—
SolventDimethylformamideHCID 6228—
Product3-[4-(3-Bromo-phenylamino)-quinazolin-7-ylcarbamoyl]acrylic acid ethyl esterHCID 5370151223.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

To an ice cold solution of 0.158 g of 7-amino-4(3-bromoanilino)-quinazoline and 0.216 g of monoethyl fumarate in 3 mL of dry dimethylformamide was added 0.288 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide HCl (EDAC). 7-Amino-4-(3-bromoanilino)quinazoline can be made by methods well-known to those skilled in the art. See, for example, J Med Chem, 1995:3482, which is hereby incorporated by reference. After stirring at 5° C. for 5 minutes, the ice bath was removed, and the reaction was permitted to warm to room temperature where it stirred for 15 hours. The reaction was poured into cold water, and the suspension was made basic with the addition of a saturated sodium bicarbonate solution. The resulting solid was collected by filtration, washed with water, and then recrystallized from 50 mL of ethanol to afford 0.052 g of the desired product, mp >260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344459B1
Source datasetuspto-grants-2002_02
ORD IDord-fe4d16ab9b75447683ce20a5502c1efc
Source noteuspto-grants-2002_02