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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401502Generated: October 30, 2026

2-(Dimethylamino)ethanol → HCID 57690626, compound

https://huagongshe.com/reaction/401502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantLithiumHCID 3028194—
Reactant2-Fluoro-N-methoxy-N-methylnicotinamideHCID 53417067—
Reactanttert-Butyl 4-(isoquinolin-3-yl)piperazine-1-carboxylateHCID 57690803—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57690626HCID 576906268%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2-dimethylaminoethanol (0.072 ml, 0.72 mmol) in hexanes (3 ml) was cooled down to −40° C. A 2.5M solution of nbutyl lithium in tetrahydrofuran (0.574 ml, 1.44 mmol) was added dropwise. The solution was stirred for 20 minutes. A suspension of tert-butyl 4-(isoquinolin-3-yl)piperazine-1-carboxylate (0.75 mg, 0.24 mmol) in hexanes (8 ml) was added and the resulting solution was stirred for 1 hour. The solution was cooled down to −78° C. A solution of 2-fluoro-N-methoxy-N-methylnicotinamide (176.3 mg, 0.96 mmol) in THF (40 ml) was added dropwise. The reaction mixture was warmed up to −50° and stirred for 1 hour, then the mixture was stirred at 0° C. for a further 1 hour. The crude mixture was partitioned between water and ethyl acetate. The organic extract was dried over magnesium sulfate, filtered and concentrated under vacuo. The residue was and purified on silica gel by flash column chromatography to give the title compound as a yellow oil (8 mg, 8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741931B2
Source datasetuspto-grants-2014_06
ORD IDord-c1d12809e815467b9afc7a8a7d9b42db
Source noteuspto-grants-2014_06