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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532111Generated: October 26, 2026

4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamide → 4-(2-Allyloxybenzamido)-1-methyl-3-n-propyl-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1532111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamideHCID 3338044—
Reactant2-[(Prop-2-en-1-yl)oxy]benzoyl chlorideHCID 12593892—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product4-(2-Allyloxybenzamido)-1-methyl-3-n-propyl-pyrazole-5-carboxamideHCID 5363906866.1%

Reaction Steps

A solution of 2-allyloxybenzoyl chloride (3.93 g, 0.02 mol) in dichloromethane (20 ml) was added dropwise to a stirred, partial solution of 4-amino-1-methyl-3-n-propylpyrazole-5-carboxamide (3.64 g, 0.02 mol) in pyridine (50 ml), and the resulting mixture stirred at room temperature overnight in a dry atmosphere. The solvent was evaporated under vacuum and the residue partitioned between dichloromethane (50 ml) and saturated aqueous sodium carbonate solution (50 ml). The organic layer was separated and the aqueous layer exhaustively extracted with further dichloromethane. The combined organic solutions were washed with 2M Hcl (3×30 ml), then brine (1×30 ml), and dried (Na2SO4). After filtration and evaporation under vacuum of the filtrate, the crude product was crystallised from ethyl acetate to give the title compound (4.525 g, 66%), m.p. 132-134° C. Found: C, 63.49; H, 6.42; N, 16.33. C18H22N4O3 requires C, 63.14; H, 6.48; N, 16.36%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200980B1
Source datasetuspto-grants-2001_03
ORD IDord-bdf239cc51f743bdb1497d6fd021e44e
Source noteuspto-grants-2001_03