HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethylamine → [1-(2-Amino-ethyl)-6-chloro-1H-indol-3-yl]-[4-(2-trifluoromethoxy-phenyl)-piperidin-1-yl]-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethylamine | HCID 13369 | — |
| Reactant | (6-chloro-1H-indol-3-yl)-[4-(2-trifluoromethoxy-phenyl)-piperidin-1-yl]-methanone | HCID 59429664 | — |
| Product | [1-(2-Amino-ethyl)-6-chloro-1H-indol-3-yl]-[4-(2-trifluoromethoxy-phenyl)-piperidin-1-yl]-methanone | HCID 59429642 | — |
Reaction Steps
Analogous to general procedure II, the alkylation of (6-chloro-1H-indol-3-yl)-[4-(2-trifluoromethoxy-phenyl)-piperidin-1-yl]-methanone (prepared herein) with (commercially available) 2-chloro-ethylamine gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781436B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-d08b5d7b960e4fc3a72990f3c5bf777d |
| Source note | uspto-grants-2010_08 |