HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → HCID 59238948, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | 1-Boc-3-pyrrolidinol | HCID 4416939 | — |
| Reactant | HCID 67211699 | HCID 67211699 | — |
| Product | HCID 59238948 | HCID 59238948 | — |
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 3-hydroxypyrrolidine-1-carboxylate. 1H-NMR (400 MHz, CDCl3) δ ppm 9.26 (br s, 2 H), 8.35 (s, 1 H), 8.06 (d, J=1.2 Hz, 2 H), 7.39-7.29 (m, 4 H), 5.11 (t, J=3.8 Hz, 1 H), 3.60-3.50 (m, 1 H), 3.34 (d, J=11.6 Hz, 1 H), 3.20 (td, J=10.2, 4.0 Hz, 1 H), 2.88 (dd, J=12.2, 3.2 Hz, 1 H), 2.40-2.30 (m, 1 H), 2.22-2.10 (m, 1 H); MS (ESI) m/z 408.1 (M−H)−; MS (ESI) m/z 410.0 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399502B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-624e93af760247d4bc3a554506d03f4a |
| Source note | uspto-grants-2013_03 |