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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394730Generated: October 29, 2026

Methacrylic Acid → HCID 18176145, compound

https://huagongshe.com/reaction/394730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant7-Amino-4-[(3-bromophenyl)amino]quinazolineHCID 5328045—
SolventDimethylformamideHCID 6228—
ProductHCID 18176145HCID 1817614524%

Reaction Steps

To a stirred solution of 7-amino-4-[(3-bromo-phenyl)amino]quinazoline (J Med Chem, 1995;38:3482) (150 mg, 0.48 mmol) in dry DMF (20 mL) was added methacrylic acid (200 mg) and 1-(3-dimethylamino-propyl)-3-ethylcarbodiimide hydrochloride (EDCI.HCl) (2.5 mol, 228 mg), the reaction mixture was stirred overnight then further amounts of EDCI.HCl (230 mg) and methacrylic acid (200 mg) were added. After a further 2 days stirring the solvent was removed under vacuum and the residue diluted with saturated NaHCO3, extracted with ethyl acetate (EtOAc) and then the combined organic extracts were dried over anhydrous Na2SO4, concentrated under reduced pressure and chromatographed on silica gel eluting with MeOH/CH2Cl2/EtOAc (5:45:50) to MeOH/CH2Cl2/EtOAc (10:40:50) to give N-[4-[(3-bromophenyl)amino]-quinazolin-7-yl]-2-methyl-acrylamide (43 mg, 24%) as a pale brown solid, mp (CH2Cl2/hexane) 255-259° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602863B1
Source datasetuspto-grants-2003_08
ORD IDord-f1b930bc3cec4be283f94caebebd2ee4
Source noteuspto-grants-2003_08