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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701970Generated: October 31, 2026

Potassium Carbonate → HCID 20504611, compound

https://huagongshe.com/reaction/1701970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclohexyl isocyanateHCID 18502—
ReactantHCID 20504601HCID 20504601—
ReactantHCID 20504610HCID 20504610—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 20504611HCID 20504611—

Reaction Steps

1.2 g N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-cyclohexyl-thio-urea (m.p. 179°-181° C., prepared from 4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonamide and cyclohexyl-isocyanate in acetone in the presence of potassium carbonate) are dissolved in 75 ml of acetone and 10 ml of water. At 0° C., a solution of 0.1 g of sodium nitrite in 5 ml of water is added to this solution, subsequently 0.8 ml of 5 N acetic acid is added dropwise, and agitation is continued for 2 hours at 0° C. Subsequently, the acetone is evaporated under reduced pressure, the product is suction-filtered and reprecipitated from dilute ammonia. After recrystallization from dilute acetone, N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-cyclohexyl urea has a melting point of 176°-178° C., and with the product prepared according to Example 8, shows no depression.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379785
Source datasetuspto-grants-1983_04
ORD IDord-316cc090158345e089273f5a6e3bcfd3
Source noteuspto-grants-1983_04