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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736882Generated: October 27, 2026

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

https://huagongshe.com/reaction/736882

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 numberUS07595405B2
Source datasetuspto-grants-2009_09
ORD IDord-54d157d363e84f529c0b9aa8e6ef2a02
Source noteuspto-grants-2009_09