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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188550Generated: October 31, 2026

HCID 49764568, compound → HCID 49764569, compound

https://huagongshe.com/reaction/2188550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 49764568HCID 49764568—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 49764569HCID 49764569—

Reaction Steps

N-({1-[4-(5-Bromo-2-oxo-2H-pyrimidin-1-yl)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide (as prepared in Example 3, Step C, ˜150 mg, 0.27 mmol) in MeOH (20 mL) was driven through H-Cube® Continuous-flow Hydrogenation reactor (ThalesNano, Budapest, Hungary) under full hydrogen mode at room temperature using 10% Pd/C cartridge. The resulting solution was concentrated and purified by silica gel column on a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324186B2
Source datasetuspto-grants-2012_12
ORD IDord-5ebcdeb866fa4b4880e64ae1762a0ea6
Source noteuspto-grants-2012_12