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ChemicalBook CAS DataBase List 5-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine

5-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine synthesis

6synthesis methods
1312755-43-3 Synthesis
2-PyridinaMine, 5-broMo-3-(1-propyn-1-yl)-

1312755-43-3
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Yield: 97%

Reaction Conditions:

with potassium tert-butylate in tert-butyl alcohol at 85; for 1 h;

Steps:


Step 3 : 5-Bromo-2-methyl-lH-pyrrolor2,3-b1pyridine5-Bromo-3-prop-l-ynyl-pyridin-2-ylamine (91 g, 431 mmol) was treated with a 1M solution of potassium ie/t-butoxide in ie/t-butanol (700 mL) and the reaction mixture was heated at 85 °C for 1 hour. The mixture was then allowed to cool to ambient temperature and poured onto a 1: 1 mixture of water / ice {ca. 1 L). The resultant precipitate was collected by filtration, washed with water and left to air dry. The resultant solid was dissolved in dichloromethane, dried (Na2S04) and evaporated then triturated with diethyl ether to afford the title compound as a brown solid (88.7 g, 97%). NMR (400 MHz, CDC13): 10.21 (s, 1H), 8.22 (d, J = 2.1 Hz, 1H), 7.91 (d, J = 2.1 Hz, 1H), 6.13 (s, 1H),2.52 (s, 3H).

References:

F. HOFFMANN-LA ROCHE AG;DYKE, Hazel Joan;GAZZARD, Lewis J.;WILLIAMS, Karen WO2011/73263, 2011, A1 Location in patent:Page/Page column 79

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