Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4-Methoxy[2,2′-bipyridine]-6-carbonitrile | HCID 13586798 | — |
| Catalyst | HCID 86707187 | HCID 86707187 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67608342 | HCID 67608342 | — |
Reaction Steps
A mixture of 4-Methoxy-[2,2′]bipyridinyl-6-carbonitrile (1.0 g, 4.73 mmol), Palladium hydroxide-Pd 20%-50% in water (0.66 g, excess), ammonium formate (1.5 g, excess) and ethanol (60 mL) was stirred at 27° C. for 2 hours. The reaction was then filtered thorough celite, washed with methanol (150 mL) and dichloromethane (150 mL) and the organic phase evaporated to dryness affording C-(4-Methoxy-[2,2′]bipyridinyl-6-yl)-methylamine as an orange oil (0.80 g, 45%, in a ratio 72 to 28 product vs. byproduct).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284296B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-10b15ff6da5b48f09413dff1e52b33f7 |
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| Source note | uspto-grants-2016_03 |
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