Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820443Generated: October 30, 2026

1-Phenylethanol → HCID 68681896, compound

https://huagongshe.com/reaction/1820443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylethanolHCID 7409—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant(Cyanomethyl)trimethylphosphonium chlorideHCID 57431663—
Reactant(4,4-Difluoro-piperidin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanoneHCID 68680853—
SolventTolueneHCID 1140—
ProductHCID 68681896HCID 68681896—

Reaction Steps

The title compound was synthesized in analogy to example 74, from (cyanomethyl)trimethylphosphonium chloride (prepared according to Tetrahedron Lett. 1996, 37 (14), 2459-62), potassium bis(trimethylsilyl)amide, 1-phenylethanol and (4,4-difluoro-piperidin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone (example 32) in toluene, to give the compound as a light brown foam (37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601711B2
Source datasetuspto-grants-2009_10
ORD IDord-55d665f66075463aa9ce8978b5877031
Source noteuspto-grants-2009_10