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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472909Generated: October 30, 2026

Bicyclo[2.2.1]hept-2-en-2-ylboronic acid → HCID 68312873, compound

https://huagongshe.com/reaction/1472909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicyclo[2.2.1]hept-2-en-2-ylboronic acidHCID 44119810—
ReactantHCID 68312512HCID 68312512—
CatalystPalladiumHCID 23938—
ProductHCID 68312873HCID 68312873—
ProductHCID 131732758HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012651B2
Source datasetuspto-grants-2015_04
ORD IDord-22f6137c6c0e47aebf9fa19d941b3435
Source noteuspto-grants-2015_04