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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669533Generated: October 31, 2026

Sodium Iodide → N-(1-(3,4-dichlorophenyl)-1H-pyrazol-3-yl)-2-morpholinoacetamide

https://huagongshe.com/reaction/1669533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant2-chloro-N-(1-(3,4-dichlorophenyl)-1H-pyrazol-3-yl)acetamideHCID 57705413—
SolventDimethylformamideHCID 6228—
ProductN-(1-(3,4-dichlorophenyl)-1H-pyrazol-3-yl)-2-morpholinoacetamideHCID 2474357087.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-chloro-N-(1-(3,4-dichlorophenyl)-1H-pyrazol-3-yl)acetamide (0.22 g, 0.74 mmol), morpholine (71 mg, 0.81 mmol), potassium carbonate (0.22 g, 1.62 mmol) and sodium iodide (0.11 g, 0.74 mmol) in dry dimethylformamide (5 ml) was stirred and warmed at 100° C., overnight, in a dry nitrogen atmosphere. The solvent was evaporated in vacuo and water was added to the crude residue. The dark solid precipitated was filtered and dried yielding a crude product purified by crystallization in ethyl acetate, and 0.23 g of N-(1-(3,4-dichlorophenyl)-1H-pyrazol-3-yl)-2-morpholinoacetamide was obtained as a beige colour solid with m.p.=125-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989485B2
Source datasetuspto-grants-2011_08
ORD IDord-b5ac432c7e7d4090aa67d1cd0bdfdc73
Source noteuspto-grants-2011_08