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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839228Generated: October 25, 2026

Phosphorus oxychloride → 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/839228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonyl chlorideHCID 20325933—
Reactant3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 20325964—
Solvent1,1-DichloroethaneHCID 6365—
Product3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamideHCID 20326123—

Reaction Steps

Heat 1 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid together with 0.56 g of phosphorus oxychloride and 10 ml of dichloroethane for 2 hours at 80° C. Add 10 ml of a 25% aqueous solution dropwise at 0° C to the thus-obtained solution of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic chloride. Allow the resulting mixture to stand overnight and then vacuum distil it to remove the organic solvent therefrom. Vacuum filter to separate formed precipitate and recrystallize the filter residue from dimethylformamide/methanol to obtain 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxamide [m.p. 236° to 238° C].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093812
Source datasetuspto-grants-1978_06
ORD IDord-5d8967682a2c4ddfacb5de96cc45fbc9
Source noteuspto-grants-1978_06