HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(5-chloro-[1H]-indol-3-yl)-piperidine → HCID 131724868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(5-chloro-[1H]-indol-3-yl)-piperidine | HCID 12831375 | — |
| Reactant | HCID 12992363 | HCID 12992363 | — |
| Product | HCID 131724868 | HCID 131724868 | — |
Reaction Steps
from 5-chloro-3-(piperidin-4-yl)-1H-indole and 1-(3-bromopropan-1-yl)-3,4-dihydroquinolin-2(1H)-one. Mp 142-146° C. 1H NMR (DMSO-d6): 1.95-2.15 (m, 6H); 2.60 (t, 2H); 2.90 (t, 2H); 2.95-3.15 (3H); 3.15-3.20 (m, 2H); 3.55 (d, 2H); 3.95 (t, 2H); 7.00-7.10 (m, 2H); 7.20-7.30 (m, 4H); 7.35 (d, 1H); 7.75 (s, 1H), 11.30 (broad s, 1H); 11.15 (s, 1H). MS m/z: 422 (MH+), 188.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276508B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-bfa290c1b45c4f28a10bff5fa5715ba9 |
| Source note | uspto-grants-2007_10 |