HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21197810, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Reactant | 3,7-dichloro-2H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 12700105 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21197810 | HCID 21197810 | 59% |
Reaction Steps
To a solution of O-benzylhydroxylamine hydrochloride (500 mg) and triethylamine (200 mg) in ethanol (10 ml) was added 3,7-dichloro-4H-1,2,4-benzothiadiazine 1,1-dioxide (500 mg). The mixture was stirred for 3 h and concentrated in vacuo. The crude product was taken up in hot ethyl acetate (50 ml) and cooled to room temperature and the precipitate was collected by filtration to give the title compound (200 mg, 59%); m.p. >220° C.; 1H-NMR (DMSO-d6) ppm; 11.2 (br s, 1H, NH), 7.7-7.35 (m, 9H, arom. and NH), 4.49 (s, 2H, CH2). Analysis: C14H12ClN3O3S requires C, 49.78; H, 3.58; N, 12.44; (found C, 49.49; H, 3.80; N, 12.09).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242443B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-1962b9d53b6449ec815bcceb96d90d9d |
| Source note | uspto-grants-2001_06 |