HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-1-(2,3-dihydro-1H-indol-1-yl)butan-1-one → 4-[4-(3-Chlorophenyl)piperazin-1-yl]-1-(2,3-dihydro-1H-indol-1-yl)butan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-1-(2,3-dihydro-1H-indol-1-yl)butan-1-one | HCID 3598062 | — |
| Reactant | 1-(3-Chlorophenyl)piperazine dihydrochloride | HCID 11957487 | — |
| Product | 4-[4-(3-Chlorophenyl)piperazin-1-yl]-1-(2,3-dihydro-1H-indol-1-yl)butan-1-one | HCID 11952831 | — |
Reaction Steps
from 1-(3-chlorophenyl)piperazine, dihydrochloride and 4-chloro-1-(2,3-dihydro-1H-indol-1-yl)butan-1-one. Mp 102–107° C. 1H NMR (DMSO-d6): 1.75–1.85 (m, 2H); 2.35 (t, 2H); 2.45–2.55 (m, 6H); 3.10–3.20 (m, 6H); 4.10 (t, 2H); 6.75 (d, 1H); 6.85 (d, 1H); 6.90 (s, 1H); 6.95 (t, 1H); 7.10 (t, 1H); 7.15–7.25 (m, 2H); 8.10 (d, 1H). MS m/z: 384 (MH+), 265, 188.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223765B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-b45953118af84d75b6dc46d9cc2efa40 |
| Source note | uspto-grants-2007_05 |