Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 21386599 | HCID 21386599 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86735385 | HCID 86735385 | — |
Reaction Steps
Milliliter of acetyl chloride was added dropwise, while stirring and cooling with an ice mixture, to a solution of 1.36 g of 3-carbomethoxyamino-7-(3-trifluoromethyl-phenylsulfonyloxy)-1H-2,1,4benzothiadiazine in 20 ml of pyridine. After the mixture had been stirred for 2 hours at 0° C, 1 ml of acetyl chloride was added once more. After another hour of stirring at 0° C, the reaction mixture was diluted with water. It was then shaken with ethyl acetate, and the extract was washed with saturated sodium chloride solution. After evaporation of the solvent, the residue was isolated by trituration with methanol and filtration. 1-Acetyl-3-carbomethoxy-amino-7-(3-trifluoromethyl-phenylsulfonyloxy)-1H-2,1,4-benzothiadiazine was obtained in a yield of 1.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04069325 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-06901f1a17e74b018ad187f5cf921fb2 |
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| Source note | uspto-grants-1978_01 |
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