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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811056Generated: November 1, 2026

4-(Dimethylamino)benzoic acid → HCID 59374991, compound

https://huagongshe.com/reaction/1811056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Dimethylamino)benzoic acidHCID 12092—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromo-o-toluidineHCID 123538—
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59374991HCID 5937499153.5%

Reaction Steps

A suspension of 4-(dimethylamino)benzoic acid (100 mg, 0.605 mmol) in DCM (3 mL) was treated with 1-chloro-N,N,2-trimethylprop-1-en-1-amine (0.120 mL, 0.908 mmol) and the resulting solution was stirred at rt for 1.5 h. 3-Bromo-2-methylaniline (0.053 mL, 0.432 mmol) was added, followed by DIEA (0.264 mL, 1.513 mmol). The mixture was stirred at rt for 1 h, then was diluted with DCM and NaHCO3 (aq). The layers were separated and the organic phase was washed with brine, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 85:15 to 65:35 hexane-EtOAc) to provide N-(3-bromo-2-methylphenyl)-4-(dimethylamino)benzamide as a light yellow solid (77 mg, 53%). 1H NMR (400 MHz, DMSO-d6) δ 9.75 (s, 1H) 7.85 (d, J=9.0 Hz, 2H) 7.49 (dd, J=8.0, 1.0 Hz, 1H) 7.30 (dd, J=7.9, 0.9 Hz, 1H) 7.15 (t, J=7.9 Hz, 1H) 6.75 (d, J=9.0 Hz, 2H) 2.99 (s, 6H) 2.25 (s, 3H). Mass spectrum m/z 331, 333 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-ff553e17ffd44c4188ad0326839cfb23
Source noteuspto-grants-2013_01