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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910978Generated: November 2, 2026

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

https://huagongshe.com/reaction/1910978

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 numberUS08604040B2
Source datasetuspto-grants-2013_12
ORD IDord-fce87613c1894846abfbb2b6e60a7a0c
Source noteuspto-grants-2013_12