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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199232Generated: October 29, 2026

Methyl iodide → N-(2,4-dichloro-thiazol-5-yl)-N-methyl-3-methylsulfanyl-propionamide

https://huagongshe.com/reaction/2199232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2,4-dichloro-thiazol-5-yl)-3-methylsulfanyl-propionamideHCID 59580948—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(2,4-dichloro-thiazol-5-yl)-N-methyl-3-methylsulfanyl-propionamideHCID 5958078844%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of N-(2,4-dichloro-thiazol-5-yl)-3-methylsulfanyl-propionamide (596 mg, 2.2 mmol) in DMF (11 mL) stirring at 25° C. was added K2CO3 (365 mg, 2.64 mmol) and iodomethane (375 mg, 1.2 mmol), the solution was stirred at 25° C. for 20 h. The solution was diluted with 50 mL H2O and extracted with ethyl acetate (3×20 mL). The combined organic extracts were washed with H2O (3×20 mL), dried over Na2SO4, filtered and concentrated to dryness under reduced pressure. The crude product was purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes) to give the desired product as a clear oil (273 mg, 44%): 1H NMR (300 MHz, CDCl3) δ 3.23 (s, 3H), 2.79 (t, J=7.2 Hz, 2H), 2.52 (t, J=7.2 Hz, 2H), 2.09 (s, 3H); ESIMS m/z 285.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09357780B2
Source datasetuspto-grants-2016_06
ORD IDord-154d733d5ba247edbedda50a63dbcbc5
Source noteuspto-grants-2016_06