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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958882Generated: October 29, 2026

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

https://huagongshe.com/reaction/1958882

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 numberUS08410159B2
Source datasetuspto-grants-2013_04
ORD IDord-52f897bef7384d609ac7015eafa40d33
Source noteuspto-grants-2013_04