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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093466Generated: November 1, 2026

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

https://huagongshe.com/reaction/2093466

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 numberUS08445499B2
Source datasetuspto-grants-2013_05
ORD IDord-a9b17a5298cc4bb3ae23c18e5b2970f5
Source noteuspto-grants-2013_05