HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicyclo[2.2.1]hept-2-en-2-ylboronic acid → HCID 68312873, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicyclo[2.2.1]hept-2-en-2-ylboronic acid | HCID 44119810 | — |
| Reactant | HCID 68312512 | HCID 68312512 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 68312873 | HCID 68312873 | — |
| Product | HCID 131732758 | HCID 131732758 | — |
Reaction Steps
(R)-tert-butyl 5-fluoro-6-4(1-hydroxy-3-methylbutan-2-yl)amino)methyl)-5′,6′-dihydro-[2,3′-bipyridine]-1′(2′H)-carboxylate was prepared according to Example 199, substituting tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate for bicyclo[2.2.1]hept-2-en-2-ylboronic acid. (R)-tert-butyl 5-fluoro-6-(((1-hydroxy-3-methylbutan-2-yl)amino)methyl)-5′,6′-dihydro-[2,3′-bipyridine]-1′(2′H)-carboxylate was subjected to hydrogenation (H2 atmosphere, Pd/C catalyst) to provide the title compound. MS (ESI+) m/z 396 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012651B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-22f6137c6c0e47aebf9fa19d941b3435 |
| Source note | uspto-grants-2015_04 |