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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251272Generated: November 2, 2026

Dimethylformamide → HCID 22502878, compound

https://huagongshe.com/reaction/1251272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22502986HCID 22502986—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22502878HCID 2250287852.7%

Reaction Steps

A solution of 4-(4-ethylpiperidin-1-yl)-3-bromoisoquinoline (1.03 g) in tetrahydrofuran (20 ml) was cooled to −78° C., followed by the dropwise addition of 1.7M tert-butyllithium (3 ml). Fifteen minutes later, N,N-dimethylformamide (0.5 ml) was added thereto and the temperature of the reaction solution was raised to room temperature. To the reaction solution was added an aqueous solution of ammonium chloride, and the mixture was extracted with ethyl acetate, followed by washing with water and brine, drying and evaporating. The resulting residue was dissolved in methanol (15 ml), and reacted with sodium borohydride (0.4 g). The solvent was removed, the resulting residue was extracted with ethyl acetate extraction, followed by washing with water and brine, drying and evaporating. The resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give 4-(4-ethylpiperidin-1-yl)-3-hydroxymethylisoquinoline (0.46 g, 52.7%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-ddfb363f0a434a5a8d8794c0bbcd4543
Source noteuspto-grants-2002_01