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98827-44-2

98827-44-2 Structure

98827-44-2 Structure
IdentificationBack Directory
[Name]

METHYL 4-HYDROXY-2H-THIENO[2,3-E]-1,2-THIAZINE-3-CARBOXYLATE-1,1-DIOXIDE
[CAS]

98827-44-2
[Synonyms]

Albb-008913
Tenoxicam Impurity 1
Tenoxicam Impurity 7
Methyl 4-hydroxy-2H-thieno[2,3-e]-1,2-thiazine-3-carboxylate...
methyl 4-hydroxy-1,1-dioxo-2H-thieno[2,3-e]thiazine-3-carboxylate
METHYL 4-HYDROXY-2H-THIENO[2,3-E]-1,2-THIAZINE-3-CARBOXYLATE-1,1-DIOXIDE
methy1 4-hydroxy-2H-thieno[2,3 -e]-1,2-thiazine-3-carboxylate-1, 1-dioxide
[EINECS(EC#)]

619-376-8
[Molecular Formula]

C8H7NO5S2
[MDL Number]

MFCD08460399
[MOL File]

98827-44-2.mol
[Molecular Weight]

261.27
Chemical PropertiesBack Directory
[Boiling point ]

464.2±55.0 °C(Predicted)
[density ]

1.716
[pka]

4.50±1.00(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Synthesis]

Methyl 3-[(methoxycarbonylmethyl)sulfamoyl]thiophene-2-carboxylate

106820-63-7

METHYL 4-HYDROXY-2H-THIENO[2,3-E]-1,2-THIAZINE-3-CARBOXYLATE-1,1-DIOXIDE

98827-44-2

General procedure for the synthesis of 4-hydroxy-2H-thieno[2,3-e]-1,2-thiazine-3-carboxylic acid methyl ester-1,1-dioxide from methyl 3-sulfonamidoacetate-2-thiophenecarboxylate: 8.5 g of methyl 3-sulfonamidoacetate-2-thiophenecarboxylic acid methyl ester (TNXK-1), 27.2 g of a 7% sodium methanol solution, and 15 mL of anhydrous methanol were mixed. The reaction was heated to reflux with stirring and maintained for 2 hours. After completion of the reaction, it was cooled to room temperature and the reaction mixture was diluted with 200 mL of water. Subsequently, the reaction mixture was neutralized with 10% hydrochloric acid solution to pH 3. After neutralization, the solvent was removed by evaporation, the residue was cooled, and the pH was adjusted again with 10% hydrochloric acid to 3. The precipitate was collected by filtration, and the filter cake was washed with water and dried to give 5.6 g of the yellowish-green solid product, 4-hydroxy-2H-thieno[2,3-e]-1,2-thiazine-3-carboxylic acid methyl ester-1,1 -dioxide (TNXK-2) The yield was 79%.

[References]

[1] Patent: CN107141308, 2017, A. Location in patent: Paragraph 0046-0050; 0064; 0068; 0074; 0078; 0084; 0088
[2] Journal of Medicinal Chemistry, 1987, vol. 30, # 4, p. 678 - 682
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