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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336842Generated: October 26, 2026

Acetonitrile → tert-butyl 4-(4-(3-(tert-butoxycarbonylamino)-5-cyano-6-(2-fluoro-4-methoxyphenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-4-yl)phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/336842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTert-butyl 4-(4-formylphenyl)piperazine-1-carboxylateHCID 2795509—
ReactantMethyl 2-fluoro-4-methoxybenzoateHCID 21255685—
Reactanttert-butyl N-(5-amino-1H-pyrazol-3-yl)carbamateHCID 45091900—
Producttert-butyl 4-(4-(3-(tert-butoxycarbonylamino)-5-cyano-6-(2-fluoro-4-methoxyphenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-4-yl)phenyl)piperazine-1-carboxylateHCID 13635299466%

Reaction Steps

To a solution of 1 g (5.18 mmol) of methyl 2-fluoro-4-methoxybenzoate in 20 ml of acetonitrile are respectively added 1.62 g (5.18 mmol) of tert-butyl 4-(4-formylphenyl)piperazine-1-carboxylate and 1.11 g (5.18 mmol) of tert-butyl 5-amino-1H-pyrazol-3-ylcarbamate. The reaction mixture is refluxed for 8 h. The solution is brought to room temperature, then the solid is filtered and rinsed several times with acetonitrile to yield 2.22 g (66%) of tert-butyl 4-(4-(3-(tert-butoxycarbonylamino)-5-cyano-6-(2-fluoro-4-methoxyphenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-4-yl)phenyl)piperazine-1-carboxylate in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889711B2
Source datasetuspto-grants-2014_11
ORD IDord-8af5f5d7677543ec98efe2308217ba68
Source noteuspto-grants-2014_11