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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914753Generated: November 2, 2026

2-Fluoro-5-iodopyridine → HCID 16748705, compound

https://huagongshe.com/reaction/914753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-iodopyridineHCID 2783179—
Reactant(2'-Methoxy[1,1'-binaphthalen]-2-yl)di(phenyl)phosphaneHCID 4190002—
Reactant(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptaneHCID 11521263—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 16748705HCID 1674870532.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl (1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (0.300 g, 1.01 mmol), prepared as described in (J. Med. Chem., (1988) 31, 1598-1611), in anhydrous toluene (30 ml) was treated with 2-fluoro-5-iodopyridine (0.34 g, 1.52 mmol), available as described in (U.S. Pat. No. 5,733,912), Pd2(dba)3 (0.028 g, 0.03 mmol), (S)-(−)-2-(diphenylphosphino)-2′-methoxy-1,1′-binaphthyl (0.028 g, 0.06 mmol), available from Strem Chemicals, and sodium tert-butoxide (0.248 g, 2.58 mmol). The reaction mixture was heated at 80° C. for 5 hours. The reaction mixture was poured into diethyl ether (100 mL), washed with brine (100 ml), dried (MgSO4), and concentrated under reduced pressure. The residue was purified by chromatography on SiO2 (3% MeOH/CH2Cl2) to provide the title compound (0.095 g, 21% yield) as a yellow oil. MS (DCI/NH3) m/z 276 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265115B2
Source datasetuspto-grants-2007_09
ORD IDord-c3c6d36e5c3c445fa8d85a05b0fad08c
Source noteuspto-grants-2007_09