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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977062Generated: November 2, 2026

2-Bromopyridine → HCID 19963216, compound

https://huagongshe.com/reaction/1977062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantSodium CarbonateHCID 10340—
Reactant(Octahydro-1H-pyrido[1,2-A]pyrazin-7-YL)methanolHCID 12985539—
SolventIsoamyl AlcoholHCID 31260—
ProductHCID 19963216HCID 1996321642%

Reaction Steps

A mixture of 1.0 g (5.9 mmol) of (7RS,9aSR)-7-hydroxymethyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (U.S. Pat. No. 5,326,874); 4.6 g (29 mmol) of 2-bromopyridine, 1.5 g (14 mmol) of sodium carbonate and 50 mL of isoamyl alcohol were refluxed for 18 h. The mixture was cooled to room temperature, filtered, and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with saturated sodium carbonate. The organic layer was dried (magnesium sulfate), filtered and evaporated, and the crude product was purified by flash chromatography on silica gel eluting first with chloroform followed by 95:5 chloroform:methanol to give 0.61 g (42%) of the title compound. 13C NMR (base, CDCl3): δ26.8, 29.0, 39.0, 45.1, 50.7, 54.8, 58.7, 60.8, 66.0, 107.1, 113.3, 137.5, 147.9, 159.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06231833B1
Source datasetuspto-grants-2001_05
ORD IDord-e96f85fb8cdf40dda905c8fb2be19d0c
Source noteuspto-grants-2001_05