HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 178527221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178509314 | HCID 178509314 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178527221 | HCID 178527221 | — |
Reaction Steps
To a solution of 7.0 g of 4-amino-7-chloro-3,4-dihydro-3-imino-1-phenyl-1,2,4-benzothiadiazine-1-oxide, prepared according to Example 6, in 250 ml tetrahydrofurane are added 0.68 g of sodium hydride (80%) in portions. After stirring for 30 minutes at room temperature 2.4 ml ethyl chloroformate, dissolved in 10 ml tetrahydrofuran, are added dropwise. The mixture is stirred at room temperature for three hours, then separated from the precipitated sodium chloride and concentrated. The residue is dissolved in 150 ml toluene and boiled for 16 hours under reflux. The precipitated product is sucked off and crystallized from dimethylformamide/methanol as colorless crystals, m. pt. 343°-348° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04612311 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-25f0743f0b0a43f7998a41c47665422a |
| Source note | uspto-grants-1986_09 |