HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 21269044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chloro-N,N-diethylacetamide | HCID 16844 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 2-amino-alpha-(hydroxyimino)thiazol-4-acetate | HCID 6401018 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21269044 | HCID 21269044 | 77.9% |
Reaction Steps
57.3 g of ethyl 2-(2-amino-4-thiazolyl)-2-(Z)-hydroxyimino-acetate, 80 g of N,N-diethylchloroacetamide, 138.7 ml of N-ethyldiisopropylamine and 80 g of sodium iodide are stirred at room temperature for 12 hours in 1.1 l of acetonitrile. The mixture is subsequently diluted with 5 l of ethyl acetate, washed with water, dried over magnesium sulphate and concentrated to a small volume. The compound which crystallizes out is filtered off and dried. There are obtained 68.1 g of ethyl 2-(2-amino-4-thiazolyl)-2-[(Z)-[(diethylcarbamoyl)methoxy]imino]-acetate of melting point 161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816582 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-6cb0964894624f7cbf5700f886139c2e |
| Source note | uspto-grants-1989_03 |