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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Amino-1-phenyl-1H-pyrazole-4-carbonitrile | HCID 2774249 | — |
| Reactant | 4-(4-Iodobenzyl)morpholine | HCID 2795500 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 67253476 | HCID 67253476 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415346B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-604f677c17474bffb0fc7c049c79ddbb |
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| Source note | uspto-grants-2013_04 |
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