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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611577Generated: October 30, 2026

Triethylamine → 5-Chloro-2-(hexahydro-1H-7a-pyrrolizinyl)furo[3,2-b]pyridine

https://huagongshe.com/reaction/611577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7a-ethynylhexahydro-1H-pyrrolizineHCID 19597695—
Reactant6-Chloro-2-iodo-3-hydroxypyridineHCID 23433158—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Product5-Chloro-2-(hexahydro-1H-7a-pyrrolizinyl)furo[3,2-b]pyridineHCID 1959762377%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001849
Source datasetuspto-grants-1999_12
ORD IDord-a36483df191c47929431d9e747c5ed7e
Source noteuspto-grants-1999_12