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188614-01-9

188614-01-9 Structure

188614-01-9 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Melting point ]

180-182°
[Boiling point ]

435.7±45.0 °C(Predicted)
[density ]

1.343±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Solid
[pka]

12.34±0.20(Predicted)
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

188614-01-9(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate(188614-01-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl thioglycolate

2365-48-2

METHYL 3-AMINO-4-IODOBENZOATE

412947-54-7

Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate

188614-01-9

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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