HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → ethyl (2Z)-2-(2-acetamido-1,3-thiazol-4-yl)-2-(2-oxopyrrolidin-3-yl)oxyiminoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Acetylthiourea | HCID 2723593 | — |
| Reactant | ethyl (2Z)-4-chloro-3-oxo-2-(2-oxopyrrolidin-3-yl)oxyiminobutanoate | HCID 13536861 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl (2Z)-2-(2-acetamido-1,3-thiazol-4-yl)-2-(2-oxopyrrolidin-3-yl)oxyiminoacetate | HCID 13536846 | 49.9% |
Reaction Steps
2.77 g of ethyl (Z)-2-[(2-pyrrolidon-3-yl)oxyimino]-3-oxo-4-chloro-n-butyrate and 1.2 g of acetylthiourea are added to 20 ml of ethanol, and 2.0 g of N,N-dimethylaniline are added thereto. The mixture is stirred at 20° to 30° C. for 4 hours. Then, the mixture is concentrated under reduced pressure to drynss. The residue is dissolved in chloroform, and the solution is washed with water and an aqueous sodium bicarbonate solution, successively. The chloroform solution is dried and concentrated under reduced pressure to remove solvent. The residue is crystallized with isopropanol, and the crystals are collected by filtration. 1.7 g of ethyl (Z)-2-(2-acetamidothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04794186 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-d6e50eb0df8941a9b773da1001eb169d |
| Source note | uspto-grants-1988_12 |