HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid | HCID 291530 | — |
| Reactant | Bistrimethylsilylacetamid | HCID 11708267 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbonyl chloride | HCID 20544473 | — |
Reaction Steps
In a similar manner to that of Example 1--1), 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbonyl chloride, which was prepared from 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid (1.8 g) and thionyl chloride (36 ml), was treated with a solution of 7-(D-2-phenylglycinamido)-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid formate (2.5 g) and bis(trimethylsilyl)acetamide (4.0 g) in methylene chloride (50 ml). Thus obtained reaction mixture was worked up in a similar manner to that of Example 1-4) to give powder (650 mg) of 7-[D-2-(4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxamido)-2-phenylacetamide]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid, mp 103° to 105° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04172198 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-5e5aaf4ab7184c74ad64c3b817474fa8 |
| Source note | uspto-grants-1979_10 |