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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-mercaptopropionate | HCID 21625 | — |
| Reactant | 2-Thiazolamine, 5-bromo- | HCID 43600 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-[(2-amino-1,3-thiazol-5-YL)sulfanyl]propanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148412B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-52e1f75ec4a54f05aa46069148dbedef |
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| Source note | uspto-grants-2012_04 |
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