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ChemicalBook CAS DataBase List 2,6-DICHLORO-4-METHOXY-PYRIDINE
17228-75-0

2,6-DICHLORO-4-METHOXY-PYRIDINE synthesis

8synthesis methods
-

Yield:17228-75-0 94%

Reaction Conditions:

with sodium hydride in N,N-dimethyl-formamide;mineral oil at 0 - 20; for 16 h;

Steps:

1 1. Preparation of 2, 6-dichloro-4-methoxypyridine
To a solution of 2,4,6-trichloropyridine (3.64 g, 20.0 mmol) in DMF (20 mL) at 0°C were slowly added NaH (60% in mineral oil, 840 mg, 21 mmol) and MeOH (673 mg, 21 mmol). The mixture was stirred at room temperature for 16 h. The mixture was concentrated and partitioned between EtOAc (30 mL) and water (15 mL). The organic extracts were dried (Na2SO4), filtered, and concentrated. The residue was purified by silica gel chromatography eluting with ethyl acetate in hexane (0-5 percent) to afford the title compound (3.0 g, yield: 94%).

References:

NEW ERA PHARMA, INC.;XIAN, Jun WO2018/106459, 2018, A1 Location in patent:Paragraph 00110

FullText

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