HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitroindoline → 2,3-dihydro-1H-indol-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitroindoline | HCID 21959507 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 2,3-dihydro-1H-indol-1-amine | HCID 2760932 | — |
Reaction Steps
Substituted indolines 51 are prepared such as by the procedures described in Scheme 15. Substituted amino-indolines 48 are prepared from the nitroindoline 46 and a ketone in the presence of NaHB(OAc)3 to form the 1-substituted indoline 47. The nitroindoline 47 is hydrogenated, such as with H2 in the presence of a catalyst, such as Pd/C, to yield the amino-indoline 48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507748B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-1587dd2df9244ca197ae4e1bfe91ec4e |
| Source note | uspto-grants-2009_03 |