HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14306449, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carzenide | HCID 8739 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 14306471 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 14306449 | HCID 14306449 | 78.5% |
Reaction Steps
To a solution of 0.48 g (2.4 mmol) of 4-sulfamoylbenzoic acid in 10 ml of DMF are added 0.29 g of Et3N and then 0.28 g ethyl chloroformate, and the mixture is stirred at room temperature for 1 hour and mixed with 0.5 g of solid 3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-one II-1. The mixture is stirred at room temperature for 2 hours, diluted with 100 ml of water and shaken with ethyl acetate. The organic layer is washed with water, dried and concentrated in vacuo. The residue is washed with ethyl acetate to give 0.68 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04840953 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-b2db750c5d8c42ae979a138e53a9491a |
| Source note | uspto-grants-1989_06 |