HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044159Generated: October 25, 2026
Potassium Carbonate → 2-(3-phenyl-propylsulfanyl)-N-(thiophen-2-yl-methyl)-pyridine-3-carboxylic acid amide
https://huagongshe.com/reaction/2044159
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, (3-iodopropyl)- | HCID 138121 | — |
| Reactant | 2-mercapto-N-(thiophen-2-ylmethyl)nicotinamide | HCID 178523048 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-phenyl-propylsulfanyl)-N-(thiophen-2-yl-methyl)-pyridine-3-carboxylic acid amide | HCID 46908730 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586755B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-bddc698f82834eb3801e56a03fa2f73c |
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| Source note | uspto-grants-2013_11 |
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