HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-amino-N-ethylpiperidine → 3-(7-chloro-4-quinolylamino)-N-(1-ethyl-3-piperidyl)benzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-amino-N-ethylpiperidine | HCID 98094 | — |
| Reactant | Sulphonylchloride hydrochloride | HCID 19012189 | — |
| Reactant | 3-(7-Chloro-4-quinolylamino)benzenesulphonic acid | HCID 21563543 | — |
| Product | 3-(7-chloro-4-quinolylamino)-N-(1-ethyl-3-piperidyl)benzenesulphonamide | HCID 21563546 | — |
Reaction Steps
3-(7-Chloro-4-quinolylamino)benzenesulphonic acid was converted to the corresponding sulphonylchloride hydrochloride and reacted with 3-amino-1-ethylpiperidine in a similar manner to that described in Example 1 (b) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933829 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-61fe2cba52524db9906f75411af44638 |
| Source note | uspto-grants-1976_01 |