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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618342Generated: October 29, 2026

Trimethylamine → HCID 53792392, compound

https://huagongshe.com/reaction/618342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantHCID 54281356HCID 54281356—
SolventDimethylformamideHCID 6228—
ProductHCID 53792392HCID 5379239293%

Reaction Steps

N-{4-[5-(4-Chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]phenyl}-ethenesulfonamide (250 mg, 0.583 mmol) [prepared as in Example 19], was dissolved in DMF (1.1 ml). Triethylamine (0.11 ml, 0.8 mmol), followed by dimethylamine hydrochloride (36 mg, 0.69 mmol), was added and the reaction mixture was stirred for 1 h. A second batch of trimethylamine and dimethyamine hydrochloride was added and the stirring was continued overnight. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was separated and dried over sodium sulfate. The solvent was removed in vacuo and the crude product was then dissolved in ethyl acetate, after which ethanolic HCl was added to give N-{4-[5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]phenyl}-2-(dimethyl-amino)ethanesulfonamide (257 mg, 86%) as the hydrochloride salt

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05952368
Source datasetuspto-grants-1999_09
ORD IDord-16b99ccef77440a5a7c334ffba4dc09e
Source noteuspto-grants-1999_09