HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → HCID 59238986, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | HCID 22243834 | HCID 22243834 | — |
| Reactant | HCID 67211699 | HCID 67211699 | — |
| Product | HCID 59238986 | HCID 59238986 | — |
Reaction Steps
The title compound was prepared in a manner analogous to Example 28 except the starting indole is 5,7-diBOC-2,10-dichloro-6-hydroxyindolo[2,3-b]carbazole and the reagent is tert-butyl 1-(3-hydroxypropyl)piperidin-4-ylcarbamate. 1H-NMR (400 MHz, CDCl3) δ ppm 9.70 (s, 2H), 8.33 (s, 1H), 8.07 (d, J=2.0 Hz, 2H), 7.43 (d, J=8.4 Hz, 2H), 7.33 (dd, J=8.6, 2.2 Hz, 2H), 4.33 (t, J=5.4 Hz, 2H), 3.24-3.13 (m, 2H), 3.03-2.89 (m, 1H), 2.84 (t, J=6.0 Hz, 2H), 2.30-2.16 (m, 2H), 2.15-2.06 (m, 2H), 2.04-1.93 (m, 2H), 1.78-1.65 (m, 2H); MS (ESI) m/z 479.1 (M−H)−; MS (ESI) m/z 481.0 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278341B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-2558d3370c0549ff949bf5cf34be693a |
| Source note | uspto-grants-2012_10 |