HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methyl-N-(trimethylsilyl)trifluoroacetamide → HCID 14030499, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methyl-N-(trimethylsilyl)trifluoroacetamide | HCID 32510 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 13326764 | HCID 13326764 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14030499 | HCID 14030499 | — |
Reaction Steps
7β-[(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid (486 mg) was suspended in methylene chloride (9 ml), followed by an addition of N-methyl-N-(trimethylsilyl)trifluoroacetamide (980 μl). The resulting mixture was stirred at room temperature for 1 hour. After ice-cooling, iodotrimethylsilane (410 μl) was added and the resulting mixture was stirred for 15 minutes. The reaction mixture was concentrated under reduced pressure to obtain the silylated derivative of 7β-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetamido]-3-iodomethyl-3-cephem-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04748171 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-14393c7ee83841669950709502729ac5 |
| Source note | uspto-grants-1988_05 |