Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 67609763 | HCID 67609763 | — |
| Catalyst | HCID 86707187 | HCID 86707187 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67609537 | HCID 67609537 | — |
Reaction Steps
A mixture of 4-(2-Diethylamino-ethoxy)-[2,2′]bipyridinyl-6-carbonitrile (1.4 g, 5.22 mmol), Palladium hydroxide-Pd 20%-50% in water (2.25 g, excess), ammonium formate (1.65 g, excess) and ethanol (66 mL) was stirred at 27° C. for 2 hours. The reaction was then filtered thorough celite, washed with methanol (200 mL) and dichloromethane (200 mL) and the organic phase evaporated to dryness affording [2-(6-aminomethyl-[2,2′]bipyridinyl-4-yloxy)-ethyl]diethylamine as an orange oil (1.03 g, 30%, in a ratio 1 to 1 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-a280255525fc40b8acdfb9c28f94c348 |
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| Source note | uspto-grants-2016_03 |
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