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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801917Generated: October 31, 2026

Ammonia → 2-Amino-3-methoxybenzamide

https://huagongshe.com/reaction/1801917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-3-methoxybenzoic acidHCID 255720—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Amino-3-methoxybenzamideHCID 1853657176%

Reaction Steps

To 2-amino-3-methoxybenzoic acid (8.11 g, 48.52 mmmol) in DMF (150 mL) at rt were added DIEA (13.2 mL, 58.22 mmol), 2 N ammonia in MeOH (33.96 mL, 67.92 mmol), EDCI (11.16 g, 58.22 mmol), and 1-hydroxybenzotriazole (7.87 g, 58.22 mmol). The solution was stirred at rt under argon. After 20 h the solution was diluted with water and extracted ten times with EtOAc. The EtOAc volume was reduced and washed with brine. The EtOAc fraction was concentrated and diluted with diethyl ether. The resulting tan solid was collected and dried in vacuo to give 2-amino-3-methoxybenzamide (6.08 g, 76%). 1H NMR (300 MHz, DMSO-d6) δ 3.79 (s, 3H), 6.26 (bs, 2H), 6.48 (m, 1H), 6.88 (d, J=7.9 hz, 1H), 7.12 (bs, 1H), 7.19 (dd, J=8.2, 1.0 Hz, 1H), 7.70 (bs, 1H) LC-MS (ESI) m/z 167 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349851B2
Source datasetuspto-grants-2013_01
ORD IDord-4f5d8e397bcb454998756601c659529b
Source noteuspto-grants-2013_01