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ChemicalBook CAS DataBase List 6-Nitro-2H-benzo[b][1,4]thiazin-3(4H)-one
21762-74-3

6-Nitro-2H-benzo[b][1,4]thiazin-3(4H)-one synthesis

8synthesis methods
-

Yield:21762-74-3 11%

Reaction Conditions:

with sodium hydroxide in ethanol;water; for 16 h;Reflux;

Steps:

97.A Step A. 6-Nitro-2H-benzo[b][1,4]thiazin-3(4H)-one

A mixture of 2-chloro-5-nitroaniline (15 g, 87 mmol), methyl 2-mercaptoacetate (13.8 g, 130 mmol) and sodium hydroxide (10.4 g, 261 mmol) in EtOH/water (250 mL, v/v=10:1) was heated at reflux for 16 h. The reaction mixture was cooled to ambient temperature, the solvent was removed in vacuo and the residue was purified by column chromatography on silica gel (eluting with 17% EtOAc in petroleum ether) to give 6-nitro-2H-benzo[b][1,4]thiazin-3(4H)-one (2.1 g, 11%). LC/MS (Table 1, Method 2) Rt=0.790 min; MS m/z: 211 [M+H]+.

References:

US2014/206663,2014,A1 Location in patent:Paragraph 1180; 1181

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