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ChemicalBook CAS DataBase List 5-AMINO-3-BROMO-2-METHYLPYRIDINE
186593-43-1

5-AMINO-3-BROMO-2-METHYLPYRIDINE synthesis

7synthesis methods
-

Yield:186593-43-1 130 mg

Reaction Conditions:

Stage #1:5-bromo-6-methylnicotinic acid with diphenyl phosphoryl azide;triethylamine in N,N-dimethyl-formamide;tert-butyl alcohol at 100; for 2 h;
Stage #2: with hydrogenchloride in 1,4-dioxane;dichloromethane at 20; for 2 h;

Steps:

19.1 Step: 5-Bromo-6-methyl - pyridin-3-yl-amine
5-Bromo-6-methyl - pyridine-3-carboxylic acid (1 g, 4.63 mmol) wasdissolved in tert-butanol (6.6 mL) and N, N- dimethylformamide (15 mL), andthereto were added triethylamine (5.15 mL, 37.04mmol) and diphenylphosphorylazide (0.51 mL, 5.093 mmol). This mixture was heated to 100° Creaction 2h, after the end of the reaction by TLC, the solvent was evaporatedto dryness, and the residue was dissolved in saturated sodium bicarbonatesolution, extracted with ethyl acetate, dried over anhydrous sodium sulfate,filtered and the solvent was evaporated to dryness, the residue on silica gelcolumn chromatography to give a white solid. The above white solid wasdissolved in dichloromethane (10 mL), was added 4N hydrogen chloride in dioxane, stirred for 2 hours at room temperature. After completion of the reaction, the solvent was evaporated to dryness to give 5-bromo-6-methyl -pyridin-3-ylamine (white solid, 130 mg).

References:

Shanghai Pharmaceuticals Holding Co.,Ltd .;WAN, HUIXIN;LI, CHUNLI;SHI, Chen;Liu, Haiyan;Li, Ping;XIA, Guangxin;HAN, Yanan CN103420977, 2016, B Location in patent:Paragraph 0293-0296

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