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ChemicalBook CAS DataBase List 4-BROMO-3-CYANOINDOLE
903131-13-5

4-BROMO-3-CYANOINDOLE synthesis

2synthesis methods
-

Yield:903131-13-5 87%

Reaction Conditions:

Stage #1: 4-bromo-1H-indole;isocyanate de chlorosulfonyle in acetonitrile at 0; for 2.08333 h;
Stage #2: with triethylamine in acetonitrile at 0 - 20;

Steps:

14 Synthesis of 4-bromo-1H-indole-3-carbonitrile (LVII)

Example 14 Synthesis of 4-bromo-1H-indole-3-carbonitrile (LVII) To a 0° C. solution of 4-bromoindole (5 g, 25.5 mmol) in acetonitrile (50 ml) was added dropwise chlorsulfonylisocyanate (2.37 ml, 27.3 mmol) over a 5 minute period. The reaction mixture was stirred at 0° C. for 2 hours, and TEA (3.77 ml, 27.0) was added dropwise over a 10 minute period. The reaction mixture was allowed reach room temperature overnight, poured into ice/water mixture (200 ml), and the aqueous layer was extracted with EtOAc. The combined organic extracts were dried over Na2SO4, filtered, concentrated, and purified by flash chromatography to afford 4-bromo-1H-indole-3-carbonitrile LVII as an off-white solid (4.9 g, 87% yield).

References:

US2007/123527,2007,A1 Location in patent:Page/Page column 68

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