HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → HCID 58084233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | 4-Bromo-1-methyl-1H-pyrazolo(3,4-c)pyridine | HCID 57606936 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 58084233 | HCID 58084233 | — |
| Product | (4S)-1,4-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine | HCID 117678281 | — |
Reaction Steps
The requisite (4S)-1,4-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine was prepared in the following manner. Reaction of C8 at elevated temperature with trimethylboroxin in the presence of sodium carbonate and tetrakis(triphenylphosphine)palladium(0) afforded 1,4-dimethyl-1H-pyrazolo[3,4-c]pyridine. This material was reduced using the method described for synthesis of C9 from C8 in Example 2; the product was subjected to supercritical fluid chromatography to separate the enantiomers (Column: Chiral Technologies, Chiralpak IC, 5 μm; Eluent: 4:1 carbon dioxide/methanol). The second-eluting enantiomer was collected and used for synthesis of Example 20. The absolute stereochemistry was arbitrarily assigned.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145427B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ac15b1aa590743249db6449650f92439 |
| Source note | uspto-grants-2015_09 |