HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-Chloro-2-(hexahydro-1H-7a-pyrrolizinyl)furo[3,2-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7a-ethynylhexahydro-1H-pyrrolizine | HCID 19597695 | — |
| Reactant | 6-Chloro-2-iodo-3-hydroxypyridine | HCID 23433158 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | 5-Chloro-2-(hexahydro-1H-7a-pyrrolizinyl)furo[3,2-b]pyridine | HCID 19597623 | 77% |
Reaction Steps
7a-Ethynyl-hexahydro-1H-pyrrolizine from Example 15b (225 mg, 1.66 mol, 6-chloro-2-iodo-3-pyridinol (509 mg, 2.0 mmol), copper(I) iodide (60 mg, 0.30 mmol), bis(triphenylphosphine)palladium(II) chloride (58 mg, 0.08 mmol) and triethylamine (0.280 mL, 2.0 mmol) were combined in a similar fashion as that described in Example 15c. The crude product was chromatographed (silica gel; CHCl3 /MeOH, 97.5:2.5) to afford a waxy tan solid (335 mg, 77%): 1H NMR (CDCl3, 300 MHz) δ 1.88-1.97 (m, 6H), 2.21-2.33 (m, 2H), 2.67-2.79 (m, 2H), 3.19-3.26 (m, 2H), 6.70 (s, 1H), 7.14 (d, J=8.5 Hz, 1H), 7.61 (d, J=8.5 Hz, 1H); MS (CI/NH3) m/z: 263 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06001849 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-a36483df191c47929431d9e747c5ed7e |
| Source note | uspto-grants-1999_12 |