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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947665Generated: November 1, 2026

N-bromobutanimide → Tert-butyl 1'-(5-bromopyrazin-2-yl)-4,4'-bipiperidine-1-carboxylate

https://huagongshe.com/reaction/1947665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantTert-butyl 1'-pyrazin-2-yl-4,4'-bipiperidine-1-carboxylateHCID 54581959—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 1'-(5-bromopyrazin-2-yl)-4,4'-bipiperidine-1-carboxylateHCID 59178948—

Reaction Steps

The tert-butyl 1′-pyrazin-2-yl-4,4′-bipiperidine-1-carboxylate (16 mg, 0.046 mmol, prepared as described for Example 8) and N-bromosuccinimide (8.2 mg, 0.046 mmol) were dissolved in DMF (0.2 ml) and the solution stirred overnight at 50 C. The slurry was diluted with 15% brine:water (40 ml) and extracted with ethyl acetate (3×25 ml). The combined organic fraction was washed with brine, dried over magnesium sulfate, filtered, and the volatiles removed in vac. The crude material was purified by chromatography on silica gel with 20% acetone:hexanes to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399485B2
Source datasetuspto-grants-2013_03
ORD IDord-ed9f45f80f244c7ab9e91665b99fd544
Source noteuspto-grants-2013_03