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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655258Generated: October 27, 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/1655258

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 numberUS05250534
Source datasetuspto-grants-1993_10
ORD IDord-9778406cd9c54dab929b6b51ae1e6e9b
Source noteuspto-grants-1993_10