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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110151Generated: November 3, 2026

Methyl iodide → HCID 18993685, compound

https://huagongshe.com/reaction/1110151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 18993679HCID 18993679—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 18993685HCID 1899368587.1%

Reaction Steps

A mixture of 1.6 g of N-methyl-N-(2-propenyl)-2-chloro -5-(3,6-dihydro-3-methyl-4-trifluoromethyl-2,6-dioxo-1(2H)-pyrimidinyl)benzenesulfonamide (Compound #29), prepared by process C from Compound #28 and iodomethane, 100 ml of ethyl acetate and 200 mg of 5% palladium/carbon catalyst was hydrogenated in a Paar® apparatus at 28 psi of hydrogen. After 30 minutes, the catalyst was filtered and solvent removed from the filtrate by rotary evaporation. The glassy residue was treated with ethanol to give 1.4 g of the title compound as a light gray powder, m.p. 143.5°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324854
Source datasetuspto-grants-1994_06
ORD IDord-92a582b56b5c4d19a3fb8f9087512fa3
Source noteuspto-grants-1994_06