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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367417Generated: October 31, 2026

Sodium Bicarbonate → (3S,6R)-1-[2-Amino-6-(4-cyano-3-fluorophenyl)-4-pyrimidinyl]-6-methyl-N-phenyl-3-piperidinecarboxamide

https://huagongshe.com/reaction/2367417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Cyano-3-fluorophenyl)boronic acidHCID 2783130—
Reactant(3S,6R)-1-(2-Amino-6-chloro-4-pyrimidinyl)-6-methyl-N-phenyl-3-piperidinecarboxamideHCID 58504476—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(3S,6R)-1-[2-Amino-6-(4-cyano-3-fluorophenyl)-4-pyrimidinyl]-6-methyl-N-phenyl-3-piperidinecarboxamideHCID 58504588100.6%

Reaction Steps

To a solution of (3S,6R)-1-(2-amino-6-chloro-4-pyrimidinyl)-6-methyl-N-phenyl-3-piperidinecarboxamide (8 g, 23.1 mmol) in 1,4-dioxane (250 mL) was added (4-cyano-3-fluorophenyl)boronic acid (5.72 g, 34.7 mmol), Pd(PPh3)4 (2.67 g, 2.3 mmol), and sat. aqueous NaHCO3 (125 mL). The resulting mixture was refluxed overnight, cooled, and diluted with H2O (˜400 mL) to form precipitate. The mixture was filtered, and the gummy solid was dissolved in EtOAc (˜800 mL) and concentrated in vacuo to about 50 mL solvent left. The crude solution was purified by silica gel chromatography (400 g column) eluting with 20% EtOAc/hexanes to 70% EtOAc/hexanes. The fractions that contained the desired product were combined and concentrated in vacuo to afford the title compound (10 g). LC-MS (ES) m/z=431 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-d826f9bb3d1a47a6af846321c15b4cec
Source noteuspto-grants-2014_04