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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226135Generated: 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/2226135

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 numberUS05346901
Source datasetuspto-grants-1994_09
ORD IDord-5f9cfdcc1b2943e6b2628996641bdf4a
Source noteuspto-grants-1994_09