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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35937Generated: October 25, 2026

Nilutamide → 1-(4-Nitro-3-trifluoromethyl-phenyl)-3,4,4-trimethyl-2,5-imidazolidinedione

https://huagongshe.com/reaction/35937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNilutamideHCID 4493—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-(4-Nitro-3-trifluoromethyl-phenyl)-3,4,4-trimethyl-2,5-imidazolidinedioneHCID 22116922—

Reaction Steps

A solution of 3.17 g of 1-(3-trifluoromethyl-4-nitro-phenyl)-4,4-dimethyl-imidazoline-2,5-dione (French Patent No. 2,329,276) and 32 ml of dimethylformamide were added at 23° C. to 26° C. to a 50% suspension of 492 mg of sodium hydride in oil and 3 ml of dimethylformamide and after stirring for 15 minutes, a solution of 0.7 ml of methyl iodide in 2 ml of dimethylformamide was added. The mixture was stirred for 25 minutes at 24° C. to 28° C. and was then poured into 200 g of a 1--1 water-ice mixture. The mixture was extracted with ether and the organic phase was washed with saturated aqueous sodium chloride, dried, filtered and evaporated to dryness under reduced pressure to obtain 3.6 g of the desired product melting at 116° C. An analytical sample was crystallized from isopropyl alcohol to obtain 2.73 g of the product melting at 116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411981
Source datasetuspto-grants-1995_05
ORD IDord-e4df9f5c88c042ed901ecdcce32dcd67
Source noteuspto-grants-1995_05