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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947664Generated: October 28, 2026

Chlorosuccinimide → Tert-butyl 1'-(5-chloropyrazin-2-yl)-4,4'-bipiperidine-1-carboxylate

https://huagongshe.com/reaction/1947664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantTert-butyl 1'-pyrazin-2-yl-4,4'-bipiperidine-1-carboxylateHCID 54581959—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 1'-(5-chloropyrazin-2-yl)-4,4'-bipiperidine-1-carboxylateHCID 59178890—

Reaction Steps

The tert-butyl 1′-pyrazin-2-yl-4,4′-bipiperidine-1-carboxylate (64 mg, 0.19 mmol, prepared as described for Example 8) and N-chlorosuccinimide (27 mg, 0.20 mmol) were dissolved in DMF (0.9 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 10% acetone:hexanes to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399485B2
Source datasetuspto-grants-2013_03
ORD IDord-7129d04e592c42e58de4717c9b79a63d
Source noteuspto-grants-2013_03