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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633976Generated: October 25, 2026

Triethylamine → 5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amine

https://huagongshe.com/reaction/633976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methylpiperazine-1-ethylamineHCID 70284—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Amino-5-bromonicotinaldehyde hydrobromideHCID 86606146—
SolventMethanolHCID 887—
Product5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amineHCID 67154522—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (1.0 mL, 7.09 mmol) was added to a solution of 2-amino-5-bromonicotinaldehyde hydrobromide (1.0 g, 3.54 mmol) in methanol (24 mL) at room temperature. The reaction mixture was stirred for 10 minutes prior to the addition of 2-(4-methylpiperazin-1-yl)ethanamine (558 mg, 3.90 mmol). The reaction mixture was then stirred overnight and cooled to 0° C. Sodium borohydride (201 mg, 5.32 mmol) was added portionwise at 0° C. and the reaction mixture was allowed to reach room temperature and stirred for 4 hours. After concentration to dryness, the residue was purified by chromatography on silica gel using dichloromethane/methanol/ammoniac (10:0:0.1 to 9:1:0.1) as eluent. The title product was obtained as a yellow solid (560 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321769B2
Source datasetuspto-grants-2016_04
ORD IDord-42bfe850ccd542f5893df646b6f5d588
Source noteuspto-grants-2016_04