HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(5-chloro-[1H]-indol-3-yl)-piperidine → HCID 131724873, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(5-chloro-[1H]-indol-3-yl)-piperidine | HCID 12831375 | — |
| Reactant | HCID 16638840 | HCID 16638840 | — |
| Product | HCID 131724873 | HCID 131724873 | — |
Reaction Steps
from 5-chloro-3-(piperidin-4-yl)-1H-indole and 4-chloro-1-(3,4-dihydro-2H-quinolin-1-yl)butan-1-one. Mp 158-162° C. 1H NMR (DMSO-d6): 1.85-1.95 (m, 2H); 1.95-2.20 (m, 6H); 2.60-2.75 (m, 4H); 2.95-3.15 (m, 5H); 3.55 (d, 2H); 3.70 (t, 2H); 7.05-7.25 (m, 6H); 7.40 (d, 1H); 7.75 (s, 1H); 10.45 (broad s, 1H); 11.15 (s, 1H). MS m/z: 436 (MH+), 303.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276508B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-6e2f4f7e09a74a228223337b41b4a293 |
| Source note | uspto-grants-2007_10 |