Identification | More | [Name]
Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate | [CAS]
188614-01-9 | [Synonyms]
Methyl-3-Oxo-3,4-Dihydro-2H-1, Methyl 3,4-dihydro-3-oxo-2H-benzo[b][1,4]thiazine-6-carboxylate Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate Methyl 3,4-dihydro-3-oxo-2H-1,4-benzothiazine-6-carboxylate methyl 3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazine-6-carboxylate | [Molecular Formula]
C10H9NO3S | [MDL Number]
MFCD00449104 | [Molecular Weight]
223.25 | [MOL File]
188614-01-9.mol |
Hazard Information | Back Directory | [Synthesis]
GENERAL METHOD: A suspension of methyl 3-iodo-4-aminobenzoate (1 mmol), methyl thioglycolate (1.5 eq.), cuprous(I) iodide (0.05 mmol), trans-N,N'-dimethylcyclohexane-1,2-diamine (0.1 mmol), and cesium carbonate (2 eq.) in anhydrous 1,4-dioxane (4 mL) was added to a vial. Nitrogen was passed into the suspension to degas it for 3 min under stirring. Subsequently, the vial was sealed. The reaction mixture was heated at 100 °C (oil bath temperature) for 15 hours. After completion of the reaction, it was cooled to room temperature and filtered. The filtrates were combined and concentrated using a rotary evaporator and the resulting residue was purified by silica gel column chromatography (eluent: 5% dichloromethane solution in methanol) to afford the target product, methyl 3-carbonyl-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate, as a beige solid. | [References]
[1] Tetrahedron Letters, 2013, vol. 54, # 38, p. 5214 - 5216 |
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