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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57614Generated: October 26, 2026

Cesium carbonate → Tert-butyl 3,3-difluoro-5-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/57614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTricyclohexylphosphineHCID 75806—
Reactant(4-(Morpholin-4-yl)phenyl)boronic acidHCID 2795359—
ReactantTert-butyl 5-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-3,3-difluoropiperidine-1-carboxylateHCID 86717382—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
ProductTert-butyl 3,3-difluoro-5-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)piperidine-1-carboxylateHCID 71113804—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of tert-butyl 5-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-3,3-difluoropiperidine-1-carboxylate (206 mg, 0.5 mmol), 4-morpholinophenylboronic acid (207 mg, 1.0 mmol), tri(cyclohexyl)phosphine (56 mg, 0.2 mmol), Pd2(dba)3 (91 mg, 0.1 mmol) and Cs2CO3 (325 mg, 2.0 mmol) in dimethoxyethane/H2O was sealed in a microwave reaction tube and stirred at 160° C. for 80 minutes in a microwave reactor. The mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was purified by chromatography to give the title compound. MS (m/z): 541 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-748e2ead300e489bbc91e6741afdf325
Source noteuspto-grants-2016_09