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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190564Generated: October 26, 2026

4-Phenylpiperidin-4-ol → 4-Hydroxy-4-phenyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl

https://huagongshe.com/reaction/2190564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylpiperidin-4-olHCID 96387—
Reactant6-chloro-N-(5-methyl-4-phenyl-1,3-thiazol-2-yl)pyridine-3-carboxamideHCID 3379941—
Reactant4-hydroxy-4-phenyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid (5-methyl-4-phenyl-thiazol-2-yl)-amideHCID 59317978—
Reactant4-(3-trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid (5-methyl-4-phenyl-thiazol-2-yl)-amideHCID 59317981—
Product4-Hydroxy-4-phenyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinylHCID 86641502—

Reaction Steps

With a method similar to that used for the preparation of 4-(3-trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-carboxylic acid (5-methyl-4-phenyl-thiazol-2-yl)-amide, 4-hydroxy-4-phenyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-carboxylic acid (5-methyl-4-phenyl-thiazol-2-yl)-amide was prepared from 6-chloro-N-(5-methyl-4-phenyl-thiazol-2-yl)-nicotinamide and 4-phenyl-piperidin-4-ol. LCMS calcd for C27H26N4O2S (m/e) 470, obsd 471 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-bd5ad1c2c6e642459ab88f9ab2b2e2f2
Source noteuspto-grants-2012_12