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2-(3-bromo-5-methoxyphenyl)ethanamine synthesis

2synthesis methods
2-(3-bromo-5-methoxyphenyl)acetonitrile

123018-27-9
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2-(3-bromo-5-methoxyphenyl)ethanamine

262450-67-9
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Yield:262450-67-9 34.4%

Reaction Conditions:

with ammonium hydroxide in methanol; under 2585.81 Torr;Inert atmosphere;

Steps:

Preparation of compound 80-3

Compound 80-2 (1.2 g, 5.31 mmol) was dissolved in methanol (8 mL) in an autoclave at room temperature, Raney nickel (1.0 g) and concentrated ammonia (8 mL) were added. The reaction mixture was stirred overnight under a hydrogen atmosphere (50 psi). After pressure relief, the reaction solution was filtered and concentrated in vacuo to obtain compound 80-3 (420 mg, crude yield 34.4%) as a yellow oil, which was directly used in the next reaction.

References:

WO2022/63278,2022,A1 Location in patent:Page/Page column 69-70