HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylethylamine → HCID 21197856, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | 3,7-dichloro-2H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 12700105 | — |
| Product | HCID 21197856 | HCID 21197856 | — |
Reaction Steps
Starting from 3,7-dichloro-4H-1,2,4-benzothiadiazine 1,1-dioxide (753 mg; 3 mmol) and N-ethyl-N-methylamine (708 mg; 12 mmol) and with the use of same procedure as in example 21 650 mg (79%) of the title compound was prepared; m.p. >220° C.; 1H-NMR (DMSO-d6) ppm; 10.4 (s, 1H, NH), 7.69 (d, 1H, H-8), 7.61 (dd, 1H, H-6), 7.55 (d, 1H, H-5), 3.5 (q, 2H, CH2), 3.09 (s, 3H, CH3), 1.10 (t, 3H, CH3); 13C-NMR (DMSO-d6) ppm; 150.21, 134.69, 131.81, 127.27, 123.98, 121.42, 119.54, 44.2, 34.69, 11.91. Analysis C10H12ClN3O2S requires C, 43.88; H, 4.42; N, 15.35; (found C, 43.52; H 4.55; N, 15.30).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242443B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-493e88c7ba4741daabfad8826b3234a9 |
| Source note | uspto-grants-2001_06 |