Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685545Generated: October 31, 2026

Potassium Carbonate → Ethyl 3-[(2-amino-1,3-thiazol-5-YL)sulfanyl]propanoate

https://huagongshe.com/reaction/1685545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-mercaptopropionateHCID 21625—
Reactant2-Thiazolamine, 5-bromo-HCID 43600—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-[(2-amino-1,3-thiazol-5-YL)sulfanyl]propanoateHCID 57481428—

Reaction Steps

To a solution of 2-amino-5-bromothiazole (50 g, 192 mmol) in DMF (300 mL) were added potassium carbonate (53 g, 384 mmol) and ethyl 3-mercaptopropionate (25.8 g, 192 mmol). The reaction mixture was stirred at room temperature for 36 h. The mixture was partitioned between water (500 mL) and ethyl acetate (500 mL) and the isolated water phase was extracted with ethyl acetate (250 mL). The combinde organic phases were washed with water (250 mL) and 10% aqueous sodium hydrogencarbonate (250 mL), dried over anhydrous magnesium sulphate and evaporated to dryness in vacuo to give 3-(2-amino-thiazol-5-ylsulfanyl)-propionic acid ethyl ester. Yield: 19.6 g (44%). 1H-NMR (CDCl3): δ 7.07 (s, 1H); 4.15 (q, 2H); 2.88 (t, 2H); 2.61 (t, 2H); 1.26 (t, 3H); HPLC-MS: m/z: 233 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148412B2
Source datasetuspto-grants-2012_04
ORD IDord-52e1f75ec4a54f05aa46069148dbedef
Source noteuspto-grants-2012_04