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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588377Generated: October 25, 2026

Triethylamine → 4-iodo-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/588377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acidHCID 673687—
SolventDichloromethaneHCID 6344—
Product4-iodo-1-methyl-1H-pyrazole-5-carboxamideHCID 375300875%

Reaction Steps

A round-bottom flash was charged with 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid (297 g, 1.18 mol), DCM (2.97 L), and 1,1′-carbonyldiimidazole (CDI) (207 g, 97% by mass, 1.24 mol). The reaction mixture was stirred at room temperature for 45 min. Ammonium chloride (189 g, 3.53 mol) and triethylamine (498 mL, 3.53 mol) were added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and the residue was suspended in H2O (˜3 L) and granulated at room temperature for 1 h. The solid was collected via filtration, washed with H2O, and dried in a vacuum oven to afford 4-iodo-1-methyl-1H-pyrazole-5-carboxamide as a colorless solid (222 g, 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227956B2
Source datasetuspto-grants-2016_01
ORD IDord-e3bcfb06889648cbaad8ed66c541d6c7
Source noteuspto-grants-2016_01