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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888602Generated: November 2, 2026

HCID 59331975, compound → {2-(4-Chloro-phenyl)-2-[6-(3-methyl-1-trityl-1H-pyrazol-4-yl)-pyridin-3-yl]-vinyl}-methyl-(1-phenyl-ethyl)-amine

https://huagongshe.com/reaction/888602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59331975HCID 59331975—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178436102HCID 178436102—
SolventTetrahydrofuranHCID 8028—
Product{2-(4-Chloro-phenyl)-2-[6-(3-methyl-1-trityl-1H-pyrazol-4-yl)-pyridin-3-yl]-vinyl}-methyl-(1-phenyl-ethyl)-amineHCID 76753191—

Reaction Conditions

Temperature-15 °C

Reaction Steps

n-Butyllithium (0.47 ml, 0.76 mmol, 1.6M in Hexanes) was added dropwise to a solution of (R) (Diphenyl-phosphinoylmethyl)-methyl-(1-phenyl-ethyl)-amine* (0.18 g, 0.51 mmol) in dry tetrahydrofuran (9 ml) at −15° C. After 15 minutes a solution of (4-Chloro-phenyl)-[6-(3-methyl-1-trityl-1H-pyrazol-4-yl)-pyridin-3-yl]-methanone (0.14 g, 0.25 mmol) in tetrahydrofuran (0.9 ml) was added and the reaction mixture was stirred for a further 30 minutes at −15° C. before warming to room temperature over 1 hour. The reaction mixture was quenched with water, extracted with diethyl ether, organic extracts were combined, dried (MgSO4) and concentrated to afford the title compound, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247576B2
Source datasetuspto-grants-2012_08
ORD IDord-53f4b4d6d4b74882a6f3d3ca77c55683
Source noteuspto-grants-2012_08