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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206561Generated: November 1, 2026

(1,1'-Biphenyl)-2-ol → HCID 131733198, compound

https://huagongshe.com/reaction/2206561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Biphenyl)-2-olHCID 7017—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
ReactantHCID 54692957HCID 54692957—
ReactantHCID 89739691HCID 89739691—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Producttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
ProductHCID 131733198HCID 13173319881%

Reaction Conditions

Temperature100 °C

Reaction Steps

A re-sealable vial containing (S)- or (R)-3-iodo-N-(1-(tetrahydro-2H-pyran-4-yl)ethyl)pyridin-2-amine (0.333 g, 1.002 mmol), copper(I) iodide (0.0084 g, 0.044 mmol), biphenyl-2-ol (0.018 g, 0.106 mmol), and cesium carbonate (0.672 g, 2.062 mmol) was diluted with THF (3.5 mL). To the orange mixture was added ethyl 3-hydroxybut-2-enoate (0.25 mL, 1.977 mmol). The resultant blue-green contents were evacuated and purged with N2 (g) (3×). The vial was subsequently sealed and heated to 100° C. After 24 h, the reaction mixture was cooled to room temperature and filtered over a pad of Celite. The filter pad was washed with EtOAc (3×) and the filtrate was concentrated to give a thick brown oil. The resultant oil was purified on a Biotage system (50 g, gradient elution 2% EtOAc: 98% Hexanes to 15% EtOAc: 85% Hexanes, then 15% EtOAc: 85% Hexanes). The product (S)- or (R)-ethyl 2-methyl-1-(1-(tetrahydro-2H-pyran-4-yl)ethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate (0.257 g, 0.812 mmol, 81.0% yield) was isolated as a white foam. LRMS (M+H+) m/z: calcd 317.2. found 317.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-75b0620c18c34d0ebd986538353410c0
Source noteuspto-grants-2016_06