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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234616Generated: October 29, 2026

Dimethylamine → 2-Amino-5-bromo-N,N-dimethylbenzamide

https://huagongshe.com/reaction/2234616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant5-Bromoisatoic AnhydrideHCID 288561—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Product2-Amino-5-bromo-N,N-dimethylbenzamideHCID 50999512106.1%

Reaction Steps

Into an 15 mL high pressure glass vial (with Teflon screw cap) were added 5-bromoisatoic anhydride (0.401 g, 1.66 mmol), DMAP (20 mg, 0.16 mmol), and dimethylamine (2 M in THF; 5.0 mL, 10.0 mmol). The vial was sealed and placed in an oil bath at 70° C. for 8 h after which it was concentrated under vacuum. The crude product was dissolved in EtOAc and washed 2× with water followed by brine. The organic phase was dried (Na2SO4), filtered and concentrated to afford 0.428 g of 2-Amino-5-bromo-N,N-dimethyl-benzamide as a pink solid, which was used directly for the next step. 1H-NMR (500 MHz, d6-DMSO) δ=7.19 (dd, J=2.0, 8.5 Hz, 1H), 7.08 (d, J=2.0 Hz, 1H), 6.63 (d, J=8.5 Hz, 1H), 5.31 (br. s, 2H), 2.89 (br. s, 6H). MS: m/z 198/200 [C═O+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709645B2
Source datasetuspto-grants-2010_05
ORD IDord-cc94fca2db0c4493aaf51db6d2be5e70
Source noteuspto-grants-2010_05