HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-amino-N-ethylpiperidine → 4-(7-Bromo-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 | 4-(7-Bromo-4-quinolylamino)benzenesulphonic acid | HCID 21563547 | — |
| Product | 4-(7-Bromo-4-quinolylamino)-N-(1-ethyl-3-piperidyl)-benzenesulphonamide | HCID 21563534 | — |
Reaction Steps
4-(7-Bromo-4-quinolylamino)benzenesulphonic acid is converted to the corresponding sulphonyl chloride hydrochloride and reacted with 3-amino--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-72c1bb8163384ab4affdf98b3839fce1 |
| Source note | uspto-grants-1976_01 |