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443339-43-3

(5-bromopyridin-2-yl)isopropylamine synthesis

2synthesis methods
-

Yield:443339-43-3 74%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in dimethyl sulfoxide at 20 - 120; for 2 h;

Steps:

339.1 Step 1:
5-bromo-N-isopropyl-pyridin-2-amine


To a stirred solution of 5-bromo-2-fluoro-pyridine (1 g, 5.7 mmol) in DMSO (10 mL) were added propan-2-amine (2 g, 33.8 mmol) and DIEA (2.7 mL, 15.5 mmol) at room temperature.
The reaction was stirred at 120° C. for 2 h.
The resulting solution was cooled to room temperature and purified by reverse-phase column chromatography to afford the title compound (900 mg, 74% yield) as a yellow solid. LCMS (M+H)+ 215.

References:

US2018/296543,2018,A1 Location in patent:Paragraph 0717; 0718