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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731271Generated: October 25, 2026

1,1'-Carbonyldiimidazole → 5-chloro-1-methyl-N-cyclopropyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1731271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCyclopropylamineHCID 69828—
Reactant5-Chloro-1-methyl-1H-pyrazole-4-carboxylic acidHCID 2735774—
SolventTetrahydrofuranHCID 8028—
Product5-chloro-1-methyl-N-cyclopropyl-1H-pyrazole-4-carboxamideHCID 13821989116.9%

Reaction Steps

Carbonyldiimidazole (3.6 grams, 0.022 mole) was added to a solution of 5-chloro-1-methyl-1H-pyrazole-4-carboxylic acid (2.4 grams, 0.015 mole) in 40 ml. of tetrahydrofuran, and the solution was stirred at room temperature for twenty minutes. Cyclopropylamine (1.3 grams, 0.022 mole) was then added and the reaction mixture was stirred at room temperature for sixteen hours. Solvent was removed in vacuo and the residue was taken up in 250 ml. of chloroform, washed with water, washed with saturated brine, and dried using sodium sulfate and filter paper. The product was recrystallized from toluene, yielding 3.5 grams of 5-chloro-1-methyl-N-cyclopropyl-1H-pyrazole-4-carboxamide, mp=105°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04620865
Source datasetuspto-grants-1986_11
ORD IDord-d38bd1c3d665459f8a8ea4d2f94daa22
Source noteuspto-grants-1986_11