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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486749Generated: October 29, 2026

Cesium carbonate → 6-Trifluoromethyl-pyridine-2-carboxylic acid[6-(4-tert-butylcarbamoyl-piperidin-1-ylmethyl)-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/1486749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant6-Trifluoromethyl-pyridine-2-carboxylic acid (6-chloro-pyrimidin-4-yl)-amideHCID 86706565—
Reactant((4-(Tert-butylcarbamoyl)piperidin-1-yl)methyl)trifluoroborateHCID 131736817—
Catalystpalladium(II) acetateHCID 167845—
SolventOxolane--water (1/1)HCID 21881883—
Product6-Trifluoromethyl-pyridine-2-carboxylic acid[6-(4-tert-butylcarbamoyl-piperidin-1-ylmethyl)-pyrimidin-4-yl]-amideHCID 118521926—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ((4-(tert-butylcarbamoyl)piperidin-1-yl)methyl)trifluoroborate (45 mg, 0.169 mmol) in THF/water 4:1 (3 mL) are added 6-trifluoromethyl-pyridine-2-carboxylic acid (6-chloro-pyrimidin-4-yl)-amide (51.2 mg, 0.169 mmol), palladium (II) acetate, (0.949 mg, 0.00423 mmol,), X-Phos, (2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl) (4.84 mg, 0.0101 mmol) and Cs2CO3, (165 mg, 0.507 mmol). The mixture is purged with argon and is stirred overnight in a sealed tube at 80° C. The mixture is let to cool down. Water (3 mL) and AcOEt (5 mL) are added and the aqueous phase is extracted with AcOEt (10 mL). The organic phase is dried over MgSO4, filtered and evaporated. The residue is purified by prep HPLC E delivering the title compound (27 mg, 30%) as a white powder, LC-MS A: tR=0.74 min; [M+H]+=465.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428456B2
Source datasetuspto-grants-2016_08
ORD IDord-7a928ac18881410ab4577b4524703fce
Source noteuspto-grants-2016_08