HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660061Generated: October 25, 2026
2-(Phenylsulfonyl)ethanethiol → 2-[2-(benzenesulfonyl)ethylthio]-6-methyl-N-(2-thienylmethyl)-nicotinamide
https://huagongshe.com/reaction/660061
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Phenylsulfonyl)ethanethiol | HCID 447093 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-chloro-6-methyl-N-(thiophen-2-ylmethyl)nicotinamide | HCID 86628836 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-(benzenesulfonyl)ethylthio]-6-methyl-N-(2-thienylmethyl)-nicotinamide | HCID 68728234 | 64% |
Reaction Steps
336 mg (3.0 mmol) of potassium tert-butoxide were added at 0° C. to a solution of 607 mg (3.0 mmol) of 2-(phenylsulfonyl)ethanethiol in DMF (10 ml). After stirring for 10 min at 0° C., 534 mg (2.0 mmol) of 2-chloro-6-methyl-N-(thiophen-2-ylmethyl)nicotinamide were added and the mixture was then heated for 16 h at 50° C. Dilution with EA and washing with brine were then carried out. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo. CC (hexane/EA 7:3) of the residue yielded 556 mg (1.28 mmol, 64%) of 2-[2-(benzenesulfonyl)ethylthio]-6-methyl-N-(2-thienylmethyl)-nicotinamide. MS: m/z 433.1 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084470B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-0f2a74d254be4c8cb3b32ee137b20b2c |
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| Source note | uspto-grants-2011_12 |
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