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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217333Generated: October 27, 2026

N-methyl-2-pyrrolidone → 3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide

https://huagongshe.com/reaction/217333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Iodo-5-nitrobenzoic acidHCID 80580—
ReactantMethoxyisopropylamineHCID 123458—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamideHCID 5785131927.9%

Reaction Steps

EDCI (7.07 g, 36.9 mmol) was added in one portion to a stirred solution of 3-Iodo-5-nitro-benzoic acid (2.31 g, 24.6 mmol), HOBt (4.985 g, 36.9 mmol), 2-Amino-1-methoxypropane (2.73 ml, 24.6 mmol) and NMP (4.06 ml 36.9 mmol) in CH2Cl2 (120 ml) and DMF (10 ml) at 0° C. The reaction was allowed to warm to room temperature and was stirred over night. The reaction mixture was then washed with 2N NaOH, water, brine, and dried over Na2SO4. Solvent was removed in vacuo to give 2.50 g of 3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide as a yellow solid, MS (M+H)=365. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193368B2
Source datasetuspto-grants-2012_06
ORD IDord-c690305d810846cfb8ab37b4bd988111
Source noteuspto-grants-2012_06