HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → 3-Bromo-1h-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Product | 3-Bromo-1h-indole | HCID 2763277 | — |
Reaction Steps
In step 3 indole compound k undergoes bromination by treatment with N-bromosuccinimide or other bromime source (not shown) to yield 3-bromo indole compound l. Bromoindole l is then subject to oxidation in step 4 to provide dihydroindolone compound m. Compound m is a compound of formula I in accordance with the invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582760B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-1537cf4be3484571bd51d70d51c62c2d |
| Source note | uspto-grants-2009_09 |