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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834220Generated: November 2, 2026

Pyridine → HCID 86735385, compound

https://huagongshe.com/reaction/1834220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21386599HCID 21386599—
SolventWaterHCID 962—
ProductHCID 86735385HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04069325
Source datasetuspto-grants-1978_01
ORD IDord-06901f1a17e74b018ad187f5cf921fb2
Source noteuspto-grants-1978_01