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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925539Generated: October 26, 2026

Potassium Carbonate → 2-(3-phenyl-propylsulfanyl)-N-(thiophen-2-yl-methyl)-pyridine-3-carboxylic acid amide

https://huagongshe.com/reaction/1925539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, (3-iodopropyl)-HCID 138121—
Reactant2-mercapto-N-(thiophen-2-ylmethyl)nicotinamideHCID 178523048—
SolventDimethylformamideHCID 6228—
Product2-(3-phenyl-propylsulfanyl)-N-(thiophen-2-yl-methyl)-pyridine-3-carboxylic acid amideHCID 4690873069%

Reaction Steps

227 mg (1.65 mmol) of K2CO3 were added to a solution of 375 mg (1.5 mmol) of 2-mercapto-N-(thiophen-2-ylmethyl)nicotinamide in DMF (3.5 ml), and stirring was carried out for 30 min at RT. 369 mg (1.5 mmol) of 1-iodo-3-phenylpropane were then added and stirring was carried out for a further 3 d at RT. The mixture was then concentrated in vacuo and the residue was taken up in an EA/water mixture. The organic phase was separated off and the aqueous phase was extracted again with EA. The combined organic phases were dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by means of CC (EA/hex 1:1), yielding 382 mg (1.0 mmol, 69%) of 2-(3-phenyl-propylsulfanyl)-N-(thiophen-2-yl-methyl)-pyridine-3-carboxylic acid amide. MS: m/z 369.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178684B2
Source datasetuspto-grants-2012_05
ORD IDord-d059ac03ecdb4baf9ec74dae95ada73b
Source noteuspto-grants-2012_05