Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetate | HCID 581091 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 4081485 | HCID 4081485 | 65% |
Reaction Steps
2.9 ml of triethylamine were added at -10° C. to a mixture of 4.6 g of the product of Step A in 92 ml of methylene chloride and after cooling to -35° C., 6.1 g of trityl chloride were added thereto. The temperature was allowed to rise to room temperature in about 21/2 hours and the reaction mixture was washed with water and then with 0.5 N hydrochloric acid and finally with aqueous sodium acetate. The mixture was dried and evaporated to dryness. The residue was taken up in ether and the solution was concentrated to dryness again. The residue was dissolved in methanol and water and ether were added to cause crystallization. The mixture was vacuum filtered and the recovered precipitate was washed with ether to obtain 6.15 g of ethyl 2-(2-tritylamino-4-thiazolyl)-2-methoxyiminoacetate melting at 120° C. having the syn configuration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04376203 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-a9a1a43bf8fa4fd4a47c5cb12b7a3b64 |
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| Source note | uspto-grants-1983_03 |
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