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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861357Generated: October 26, 2026

Sodium Carbonate → (7S,8aS)-7-(4-Fluorophenoxy)methyl-2-(6-chloropyridazin-3-yl)-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazine

https://huagongshe.com/reaction/861357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3,6-DichloropyridazineHCID 67331—
Reactant(7RS,8aSR)-7-(4-fluorophenoxy)methyl-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazineHCID 20682345—
SolventIsoamyl AlcoholHCID 31260—
Product(7S,8aS)-7-(4-Fluorophenoxy)methyl-2-(6-chloropyridazin-3-yl)-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazineHCID 8675202566%

Reaction Steps

A mixture of 0.500 g (2.00 mmol) of (7SR,8aSR)-7-(4-fluoro-phenoxy)methyl-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazine (Preparation 3), 1.49 g (10.0 mmol) of 3,6-dichloropyridazine, and 0.508 g (4.79 mmol) of sodium carbonate in 50 mL of isoamyl alcohol was heated to reflux for 48 h. The reaction was cooled to ambient temperature, the solvent removed in vacuo, the residue taken up in ethyl acetate and water, the pH was adjusted to 11 with sodium carbonate and the layers were separated. The aqueous phase was extracted with ethyl acetate, and the combined organic layers were dried (magnesium sulfate), filtered and evaporated. Purification by flash silica gel chromatography with 90:10 ethyl acetate:hexane gave 0.478 g (66%) of the title compound. mp (.HCl) 229° C. (dec). HRMS calcd for C18 H21ClFN4O (MH+): 363.1388, found: 363.1404.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714487
Source datasetuspto-grants-1998_02
ORD IDord-b388b9834bec43e7b3f5836fde78d358
Source noteuspto-grants-1998_02