HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-(Azepan-1-yl)ethyl)piperidin-4-amine trihydrochloride → 4-m-Tolyloxy-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)-piperidin-4-yl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-(Azepan-1-yl)ethyl)piperidin-4-amine trihydrochloride | HCID 66841393 | — |
| Reactant | 4-m-tolyloxy-1H-indole-2-carboxylic acid | HCID 66841608 | — |
| Product | 4-m-Tolyloxy-1H-indole-2-carboxylic acid [1-(2-azepan-1-yl-ethyl)-piperidin-4-yl]-amide | HCID 59600129 | — |
Reaction Steps
This compound is synthesized analogously to Example 1 from 4-m-tolyloxy-1H-indole-2-carboxylic acid 133 (preparation see below) and amine 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858781B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-f8110f2e11324c52a70004d57a68489e |
| Source note | uspto-grants-2010_12 |