HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 21269052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 2-amino-alpha-(hydroxyimino)thiazol-4-acetate | HCID 6401018 | — |
| Reactant | 5-(chloromethyl)-1-methyl-1H-1,2,3,4-tetrazole | HCID 12205086 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21269052 | HCID 21269052 | 154.7% |
Reaction Steps
17.7 g of ethyl 2-(2-amino-4-thiazolyl)-2-(Z)-hydroxyimino-acetate are suspended in 320 ml of acetonitrile, treated successively with 27.6 ml of N-ethyldiisopropylamine, 16 g of 5-chloromethyl-1-methyl-tetrazole and 24 g of sodium iodide and the mixture is stirred at room temperature for 12 hours. The mixture is subsequently diluted with 1.5 l of ethyl acetate, washed three times with 500 ml of water each time, dried over magnesium sulphate and concentrated. There are obtained 39.6 g of ethyl 2-(2-amino-4-thiazolyl)-2-[(Z)-[(1-methyl-1H-tetrazol-5-yl)methoxy]imino]-acetate as an oil which is used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816582 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-15b8d17e59694e27906ea1717ed8baa5 |
| Source note | uspto-grants-1989_03 |