HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → [2,4']Bithiazolyl-5'-yl-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Methanethioamide | HCID 3005587 | — |
| Reactant | 3-Bromo-4-oxo-4-thiazol-2-yl-butyric acid ethyl ester | HCID 86587616 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [2,4']Bithiazolyl-5'-yl-acetic acid ethyl ester | HCID 68497464 | — |
Reaction Steps
To a solution of 3-bromo-4-oxo-4-thiazol-2-yl-butyric acid ethyl ester (2.2 g, 7.53 mmol) in 1,4-dioxane (40 mL) is added thioformamide (freshly made from formamide and P2S5 in 1,4-dioxane) (22.59 mmol). The mixture is refluxed overnight. The solvent is removed and NaHCO3 (aq.) (40 mL) and DCM (100 mL) are added to the residue. The organic layer is separated and the aqueous layer is extracted with DCM (2×40 mL). The combined organic layers are dried and solvent removed. The crude is purified by column (1% methanol n DCM) to give [2,4′]bithiazolyl-5′-yl-acetic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916819B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-b0093c8efa9441f4bda0fdc3d5b1ae2d |
| Source note | uspto-grants-2005_07 |