Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 28530649 | HCID 28530649 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 59253657 | HCID 59253657 | 36% |
Reaction Steps
A mixture of (1-benzyl-piperidin-4-yl)-(6-chloro-pyridazin-3-yl)-amine (D1) (3 g, 9.9 mmol), zinc cyanide (2.09 g, 17.8 mmol) and tetrakis(triphenylphosphine)palladium(0) (2.74 g, 2.3 mmol) in N,N-dimethylformamide (30 ml) was heated at 160° C. for 30 min., under microwave irradiation (Milestone MW-oven). The solvent was then evaporated in vacuo and an aqueous solution of potassium carbonate (10%) and ethyl acetate were added. The organic phase was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The residue was purified by column chromatography (silica gel; 0 to 1.5% ammonia in methanol (7M)/dichloromethane) and then by HPLC to yield D2 (1.06 g, 36%) as a solid. C17H19N5 requires 293. Found 294 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466153B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-a62e9f4807404cc9965a05a29574c2e4 |
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| Source note | uspto-grants-2013_06 |
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