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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336845Generated: October 30, 2026

tert-butyl 4-[4-[5-cyano-3-methyl-6-(2,3,6-trifluorophenyl)-2,4-dihydro-1H-pyrazolo[3,4-b]pyridin-4-yl]phenyl]piperazine-1-carboxylate → HCID 178434431, compound

https://huagongshe.com/reaction/336845

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-[4-[5-cyano-3-methyl-6-(2,3,6-trifluorophenyl)-2,4-dihydro-1H-pyrazolo[3,4-b]pyridin-4-yl]phenyl]piperazine-1-carboxylateHCID 178434166—
CatalystManganese oxideHCID 160959—
SolventDichloromethaneHCID 6344—
ProductHCID 178434431HCID 17843443175.3%

Reaction Steps

To 2.48 g (4.50 mmol) of tert-butyl 4-(4-(5-cyano-3-methyl-6-(2,3,6-trifluorophenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridin-4-yl)phenyl)piperazine-1-carboxylate diluted in 20 ml of dichloromethane are added 1.96 g (22.5 mmol) of manganese oxide. The reaction mixture is sonicated for 5 min then stirred at room temperature for 18 h. It is next filtered on Celite (cyclohexane/ethyl acetate eluent: 5:5) to yield 1.86 g of tert-butyl 4-(4-(5-cyano-3-methyl-6-(2,3,6-trifluorophenyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)phenyl)piperazine-1-carboxylate in the form of a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889711B2
Source datasetuspto-grants-2014_11
ORD IDord-d680c467feb6481fac57fd2d5c4750fd
Source noteuspto-grants-2014_11