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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093465Generated: October 31, 2026

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

https://huagongshe.com/reaction/2093465

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 Conditions

Temperature50 °C

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 numberUS08445499B2
Source datasetuspto-grants-2013_05
ORD IDord-aefc1897617245439222c862a948d26a
Source noteuspto-grants-2013_05