Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | CID 19593658 | HCID 19593658 | — |
| Reactant | N-[4-(Methylsulfanyl)phenyl]-N'-propan-2-ylsulfuric diamide | HCID 54434743 | — |
| Product | HCID 22595758 | HCID 22595758 | — |
Reaction Steps
N-(4-Methylthiophenyl)-N′-(1-methylethyl)sulfamide (4.35 g, 0.016 mol) was dissolved in dry dichloromethane (150 ml) and methanesulphonic acid (18.87 ml, 0.303 mol). The solution was cooled at 0° C. before the addition of trioxan (0.480 g, 0.005 mol) in dichloromethane (15 ml). After stirring at 0° C. for 1 hr, the reaction mixture was poured onto ice-water (250 ml), the layers separated, dried (MgSO4) and concentrated in vacuo to yield 3,4-dihydro-6-(ethylsulfonyl)-3-(1-methylethyl)-1H-2,1,3-benzothiadiazine-2,2-dioxide as a white solid. δ (1H NMR, DMSO, ppm): 0.9 (6H, d), 2.3 (3H, s), 3.9 (1H, m), 4.5 (2H, s), 6.6 (1H, d), 7.0 (2H, m), 10.1 (1H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06844338B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-c262fa680e9a43cbaf53f21acd125cd0 |
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| Source note | uspto-grants-2005_01 |
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