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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033002Generated: October 31, 2026

2-Bromomethylnaphthalene → HCID 936893, compound

https://huagongshe.com/reaction/1033002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromomethylnaphthaleneHCID 70320—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 10105052HCID 10105052—
SolventAcetonitrileHCID 6342—
ProductHCID 936893HCID 93689362.4%

Reaction Steps

A mixture of 3-amino-2-tert-butylthio-5-ethyl-6-methylpyridine (0.15 g, 0.67 mmol), 2-bromomethyl-napthalene (0.15 g, 0.67 mmol), diisopropylethylamine (86 mg, 0.67 mmol) in acetonitrile (5 mL) was refluxed under an atmosphere of nitrogen for 16 hours. The resultant mixture was concentrated under reduced pressure (15 (torr). The residue was subjected to column chromatography on silica gel (50, elution with 1% methanol in chloroform). Collection and concentration of appropriate fractions provided 98 mg (40%) of the napthylmethylaminopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308854
Source datasetuspto-grants-1994_05
ORD IDord-8809eb84f1ad4137842a7d6249b0298f
Source noteuspto-grants-1994_05