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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403198Generated: October 29, 2026

Phosphorus oxychloride → tert-Butyl 6-bromo-3',6'-dihydro-2,4'-bipyridine-1'(2'H)-carboxylate

https://huagongshe.com/reaction/403198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 4-(6-bromopyridin-2-yl)-4-hydroxypiperidine-1-carboxylateHCID 86614831—
SolventPyridineHCID 1049—
Producttert-Butyl 6-bromo-3',6'-dihydro-2,4'-bipyridine-1'(2'H)-carboxylateHCID 86614830—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 4-(6-bromopyridin-2-yl)-4-hydroxypiperidine-1-carboxylate (100 mg) in pyridine (2.5 ml) is added, at 0° C. under argon, POCl3 (0.26 ml). The mixture is stirred at 0° C. and then slowly warmed to room temperature. The mixture is stirred at room temperature overnight. The reaction mixture is subsequently admixed with saturated sodium hydrogencarbonate solution and the aqueous phase is removed. After the aqueous phase has been extracted with tert-butyl methyl ether, the combined organic phases are dried over sodium sulphate and concentrated under reduced pressure. The residue is purified by chromatography. This gives tert-butyl 6-bromo-3′,6′-dihydro-2,4′-bipyridine-1′(2′H)-carboxylate (60 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748420B2
Source datasetuspto-grants-2014_06
ORD IDord-e2d965447b0e49699427a2bb749675df
Source noteuspto-grants-2014_06