HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methyl-4-piperidyl (3S,4S)-Pivalate → HCID 59600158, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methyl-4-piperidyl (3S,4S)-Pivalate | HCID 59600241 | — |
| Reactant | HCID 66841736 | HCID 66841736 | — |
| Product | HCID 59600158 | HCID 59600158 | — |
Reaction Steps
This compound is synthesized from 4-(6-Methoxy-pyridin-3-yl)-1H-indole-2-carboxylic acid [1-(2-hydroxy-ethyl)-piperidin-4-yl]-amide (184, preparation see below) and 2,2-Dimethyl-propionic acid (3S,4S)-3-methyl-piperidin-4-yl ester (17) analogously to the method described in example 150, followed by cleavage of the protecting group.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183366B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-bc1e9b5bcf7d49e6a0c835c6828393ac |
| Source note | uspto-grants-2012_05 |