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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284440Generated: October 30, 2026

Sodium Carbonate → HCID 58084233, compound

https://huagongshe.com/reaction/2284440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTrimethylboroxineHCID 574072—
Reactant4-Bromo-1-methyl-1H-pyrazolo(3,4-c)pyridineHCID 57606936—
CatalystHCID 178418397HCID 178418397—
ProductHCID 58084233HCID 58084233—
Product(4S)-1,4-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145427B2
Source datasetuspto-grants-2015_09
ORD IDord-ac15b1aa590743249db6449650f92439
Source noteuspto-grants-2015_09