Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

914348-94-0

1-Boc-5-methyl-3-formylindole synthesis

2synthesis methods
52562-50-2 Synthesis
5-METHYLINDOLE-3-CARBOXALDEHYDE

52562-50-2
138 suppliers
$15.00/250mg

24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
839 suppliers
$13.50/25G

-

Yield:914348-94-0 0.71 g

Reaction Conditions:

with dmap in acetonitrile at 20;

Steps:

129.1 General procedure F:

General procedure: To a solution of an appropriate indole, azaindole or alternative heterocycles (1.0 eq) and di-ferf-butyl dicarbonate (1eq. to 2 eq., more in particular 1.2 eq) in acetonitrile was added DMAP (0.1 to 0.5 eq. more in particular 0.1 eq). The reaction mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in dichloromethane and washed with a saturated sodium bicarbonate solution. The phases were separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined, washed with a saturated ammonium chloride solution, water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The BOC-protected compound was used in the next step without further purification.

References:

WO2013/45516,2013,A1 Location in patent:Page/Page column 129; 182