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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Phenylsulfonyl)ethanethiolHCID 447093—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-chloro-6-methyl-N-(thiophen-2-ylmethyl)nicotinamideHCID 86628836—
SolventDimethylformamideHCID 6228—
Product2-[2-(benzenesulfonyl)ethylthio]-6-methyl-N-(2-thienylmethyl)-nicotinamideHCID 6872823464%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084470B2
Source datasetuspto-grants-2011_12
ORD IDord-0f2a74d254be4c8cb3b32ee137b20b2c
Source noteuspto-grants-2011_12