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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470416Generated: November 1, 2026

3-(Methylthio)propionyl Chloride → HCID 59580749, compound

https://huagongshe.com/reaction/1470416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylthio)propionyl ChlorideHCID 12921440—
ReactantN-methyl-2-(pyridin-3-yl)thiazol-5-amineHCID 59580894—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59580749HCID 5958074975%

Reaction Steps

A solution of 3-methylsulfanyl-propionyl chloride (120 mg, 0.9 mmol) in DCE (1 mL) was pipetted at a dropwise rate into an ice-cold suspension of methyl-(2-pyridin-3-yl-thiazol-5-yl)-amine (114 mg, 0.6 mmol) in DCE (5 mL), and the mixture was stirred for 5 min before adding a solution of DMAP (80 mg, 0.6 mmol) in DCE (1 mL). The ice bath was removed after 30 min, and the mixture was stirred at reflux under nitrogen for 15 min. The reaction mixture was cooled, diluted with DCE (70 mL), washed with saturated aqueous NaHCO3 (50 mL), dried over MgSO4 and purified by silica gel chromatography (3:1 ethyl acetate/hexanes) to afford a fine yellow powder (131 mg, 75%): mp 116-118° C.; 1H NMR (400 MHz, DMSO-d6) δ 9.08 (d, J=2.0 Hz, 1H), 8.61 (dd, J=4.8, 1.4 Hz, 1H), 8.24 (dt, J=9.8, 1.8 Hz, 1H), 7.81 (s, 1H), 7.51 (dd, J=7.7, 4.7 Hz, 1H), 3.56 (s, 3H), 3.02 (t, J=7.0 Hz, 2H), 2.76 (t, J=7.2 Hz, 2H), 2.12 (s, 3H); ESIMS m/z 294 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006446B2
Source datasetuspto-grants-2015_04
ORD IDord-4ff41118336449c9a0523a4a8f39b5c9
Source noteuspto-grants-2015_04