HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → HCID 59238883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | tert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylate | HCID 854055 | — |
| Reactant | HCID 67211699 | HCID 67211699 | — |
| Product | HCID 59238883 | HCID 59238883 | — |
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 (S)-tert-butyl 3-hydroxypyrrolidine-1-carboxylate. 1H-NMR (400 MHz, CDCl3) δ ppm 9.27 (br s, 2 H), 8.35 (s, 1 H), 8.07 (s, 2 H), 7.38-7.30 (m, 4 H), 5.09 (t, J=4.0 Hz, 1 H), 3.55-3.46 (m, 2 H), 3.29 (d, J=12.0 Hz, 1 H), 3.15 (td, J=10.0, 4.8 Hz, 1 H), 2.83 (dd, J=11.6, 3.6 Hz, 1 H), 2.38-2.28 (m, 1 H), 2.21-2.10 (m, 1 H); MS (ESI) m/z 408.2 (M−H)−; MS (ESI) m/z 410.1 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399502B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-aa4a09a077d94832bec1dee701fa0419 |
| Source note | uspto-grants-2013_03 |