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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoro-5-iodopyridine | HCID 2783179 | — |
| Reactant | (2'-Methoxy[1,1'-binaphthalen]-2-yl)di(phenyl)phosphane | HCID 4190002 | — |
| Reactant | (1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane | HCID 11521263 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 16748705 | HCID 16748705 | 32.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07265115B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-c3c6d36e5c3c445fa8d85a05b0fad08c |
|---|
| Source note | uspto-grants-2007_09 |
|---|