Identification | Back Directory | [Name]
2-METHYL-[1,2,6]THIADIAZINANE 1,1-DIOXIDE | [CAS]
137830-77-4 | [Synonyms]
2-METHYL-[1,2,6]THIADIAZINANE 1,1-DIOXIDE 2H-1,2,6-Thiadiazine, tetrahydro-2-methyl-, 1,1-dioxide 2-methyl-3,4,5,6-tetrahydro-1,2,6-thiadiazine-1,1-dioxide | [Molecular Formula]
C4H10N2O2S | [MDL Number]
MFCD06657763 | [MOL File]
137830-77-4.mol | [Molecular Weight]
150.2 |
Chemical Properties | Back Directory | [Boiling point ]
241.6±23.0 °C(Predicted) | [density ]
1.250±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
12.50±0.20(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 2-methyl-[1,2,6]thiadiazine 1,1-dioxide from 3-methylaminopropylamine was as follows: a mixture of N-methyl-1,3-propanediamine (2.06 g, 23.4 mmol) and sulfonamide (0.748 g, 7.78 mmol) was placed in a microwaveable reaction flask, sealed, and then filled with argon gas for protection. The reaction flask was stirred overnight at 50°C, and then warmed to 160°C to continue the reaction with stirring for 20 minutes. Upon completion of the reaction, the reaction mixture was concentrated and the residue was purified by column chromatography to afford 2-methyl-1,2,6-thiadiazine 1,1-dioxide (0.82 g, 70% yield). | [References]
[1] Journal of Medicinal Chemistry, 1994, vol. 37, # 19, p. 3023 - 3032 [2] European Journal of Medicinal Chemistry, 2007, vol. 42, # 9, p. 1176 - 1183 [3] Patent: WO2015/108861, 2015, A1. Location in patent: Paragraph 00401 [4] Patent: US2015/225422, 2015, A1. Location in patent: Paragraph 0555-0556 [5] Patent: US2013/303524, 2013, A1. Location in patent: Paragraph 0405-0406 |
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