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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961512Generated: November 1, 2026

2-Methyl-2-butanol → HCID 67253476, compound

https://huagongshe.com/reaction/1961512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-butanolHCID 6405—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Amino-1-phenyl-1H-pyrazole-4-carbonitrileHCID 2774249—
Reactant4-(4-Iodobenzyl)morpholineHCID 2795500—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 67253476HCID 67253476—

Reaction Conditions

Temperature100 °C

Reaction Steps

3-amino-1-phenyl-1H-pyrazole-4-carbonitrile (100 mg, 0.543 mmol), 4-(4-iodobenzyl)morpholine (165 mg, 0.543 mmol), Pd2dba3 (24.86 mg, 0.027 mmol), K2CO3 (83 mg, 0.597 mmol) and X-Phos (64.7 mg, 0.136 mmol) were added to a 5 mL microwave vial. Degassed tert-amyl alcohol (0.8 mL) was added and the vial was evacuated and back-filled with N2 (×3). The resulting mixture was stirred at 100° C. for 24 hours. Room temperature was attained, MeOH was added and the solvent removed in vacuo while loading onto silica. Purification of the residue by MPLC (0-15% MeOH—CHCl3) gave 3-{[4-(morpholin-4-ylmethyl)phenyl]amino}-1-phenyl-1H-pyrazole-4-carbonitrile as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415346B2
Source datasetuspto-grants-2013_04
ORD IDord-604f677c17474bffb0fc7c049c79ddbb
Source noteuspto-grants-2013_04