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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059170Generated: October 31, 2026

Pyridine → HCID 13036818, compound

https://huagongshe.com/reaction/2059170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl bromoacetateHCID 7748—
ReactantHCID 13036817HCID 13036817—
SolventEthylene GlycolHCID 174—
ProductHCID 13036818HCID 1303681852.8%

Reaction Steps

To 140 ml. of ethylene glycol is added 24 gm (0.08 mole) of 4-amino-3-mercapto[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]-benzene, 14 gm. (0.08 mole) ethyl bromoacetate, and 6.4 gm. (0.08 mole) of pyridine. The solution is stirred and heated at 105°-110° for 8 hours. At the end of this period the solution is cooled and poured into 800 ml of ice-water. The resultant precipitate is filtered. The precipitate is air dried and recrystallized from ethyl acetate/hexane to give 14 gm of 7-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)-ethyl]-2H-1,4-benzothiazin-3(4H)-one, m.p. 230°-232°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322417
Source datasetuspto-grants-1982_03
ORD IDord-16e63d09d3de4787bd27ce28a912be6e
Source noteuspto-grants-1982_03