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1-(5-bromopyridin-2-yl)azetidin-3-ol synthesis

1synthesis methods
53939-30-3 Synthesis
5-Bromo-2-chloropyridine

53939-30-3
462 suppliers
$5.00/1g

18621-18-6 Synthesis
3-Hydroxyazetidine hydrochloride

18621-18-6
457 suppliers
$8.00/5g

1-(5-bromopyridin-2-yl)azetidin-3-ol

1339319-85-5
7 suppliers
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Yield:1339319-85-5 5.8%

Steps:

3.4.4 5.4.4.

5.4.4.
Synthesis of 1-(5-bromopyridin-2-yl)azetidin-3-ol
To a mixture of azetidin-3-ol hydrochloride (3.3 g, 45.15 mmol) and 5-bromo-2-chloro-pyridine (8.69 g, 45.15 mmol) in DMF (50 mL) was added K2CO3 (18.72 g, 135.44 mmol), the reaction mixture was stirred at 120° C. for 3 h.
The mixture was poured into water (500 mL), extracted with EA (100 mL*3).
The organic was washed by brine (300 mL), then dried over Na2SO4 and concentrated.
The residue was purified by column chromatography to afford 1-(5-bromopyridin-2-yl)azetidin-3-ol (600 mg, 5.80% yield) as a yellow solid. MS: m/z=229.0 (M+1, ESI+).

References:

US2022/106311,2022,A1