HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 131724903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,4-Dinitrobenzaldehyde | HCID 68250 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 131724899 | HCID 131724899 | — |
| Reactant | HCID 131724904 | HCID 131724904 | — |
| Product | HCID 131724903 | HCID 131724903 | 64.2% |
Reaction Steps
7-[2-tert-butoxycarbonylmethoxyimino-2-(2-tritylaminothiazol-4-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylic acid benzhydryl ester (500 mg, 0.53 mmol), 2,4-dinitrobenzaldehyde (416 mg, 2.12 mmol), sodium iodide (79.4 mg, 0.53 mmol), triphenylphosphine (139 mg, 0.53 mmol) and sodium hydrogen carbonate (133.6 mg, 1.59 mmol) were used to conduct the procedure similar to that shown in (1) of Example 1 to obtain 350 mg (yield: 61%) of 7-[2-carboxymethoxyimino-2-(2-tritylaminothiazol-4-yl)acetamido]-3-(2,4-dinitrostyryl)-3-cephem-4-carboxylic acid benzhydryl ester as yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06897304B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-4ce50b19959e4ada9dc092e7a8e9116a |
| Source note | uspto-grants-2005_05 |