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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190562Generated: November 3, 2026

Diisopropylethylamine → 4-Hydroxy-4-phenyl-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-5'-carboxylic acid (3-iodo-4-methyl-phenyl)-amide

https://huagongshe.com/reaction/2190562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Phenylpiperidin-4-olHCID 96387—
Reactant6-chloro-N-(3-iodo-4-methyl-phenyl)-nicotinamideHCID 7925562—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,4-DioxaneHCID 31275—
Product4-Hydroxy-4-phenyl-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-5'-carboxylic acid (3-iodo-4-methyl-phenyl)-amideHCID 5931809165%

Reaction Steps

A solution of 6-chloro-N-(3-iodo-4-methyl-phenyl)-nicotinamide (100 mg, 0.26 mmol), a catalytic amount of DMAP, diisopropylethyl amine (0.14 mL, 8.1 mmol), 4-hydroxy-4-phenyl piperidine (140 mg, 8.1 mmol) in 5 mL in dioxane was heated at 95° C. in a sealed tube for about 48 h. The reaction mixture was then cooled and partitioned between EtOAc and aq. saturated Na2CO3. The organic layer was then collected, dried over Na2SO4 filtered and concentrated. The residue was chromatographed with a silica gel column and 20-100% EtOAc in hexanes to afford the product (90 mg. Yield: 65%). HRMS m/z calcd for C24H24N3O2I [M+H]+: 514.0986. Found: 514.0987.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-ca50cbd9d39047a985c9d4a5ef448b53
Source noteuspto-grants-2012_12