HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268776Generated: October 30, 2026
Methanesulfonic Acid → HCID 22595758, compound
https://huagongshe.com/reaction/2268776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 18332404 | HCID 18332404 | — |
| Reactant | CID 19593658 | HCID 19593658 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22595758 | HCID 22595758 | — |
Reaction Steps
N-(4-Ethylsulfonylphenyl)-N′-(1-methylethyl)sulfamide (5 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): 1.10 (9H, m), 3.30 (2H, q), 4.10 (1H, m), 4.80 (2H, s), 6.95 (1H, d), 7.75 (1H, dd), 7.80 (1H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06329366B1 |
|---|
| Source dataset | uspto-grants-2001_12 |
|---|
| ORD ID | ord-63a0404d961b497d9c4bf7a75b9c2046 |
|---|
| Source note | uspto-grants-2001_12 |
|---|