Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 10081254 | HCID 10081254 | — |
| Product | HCID 13533705 | HCID 13533705 | — |
Reaction Steps
A 90 mg portion of 6-chloro-3,3'-bipyridine and 0.15 ml of anhydrous hydrazine were dissolved in 20 ml of pyridine and heated at 110° C. for 48 hours. The volatiles were removed at reduced pressure and the residue dissolved in 20 ml of triethyl orthoacetate and heated at 110° C. for 12 hours. The volatiles were removed at reduced pressure and the residue purified by chromatography on silica gel, eluting with ethyl acetate:methanol (9:2). The obtained tan solid was recrystallized from ethyl acetate-methanol, giving the desired product as off-white flakes, mp 199°-201.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04550166 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-5523593def274018af4d0ba2088e1ee8 |
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| Source note | uspto-grants-1985_10 |
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