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128200-30-6

Spiro[1-azabicyclo[2.2.2]octane-3,5'(4'H)-oxazole], 2'-(1-methyl-1H-indol-3-yl)-, (-)- synthesis

3synthesis methods
19012-03-4 Synthesis
1-Methylindole-3-carboxaldehyde

19012-03-4
211 suppliers
$6.00/1g

Spiro[1-azabicyclo[2.2.2]octane-3,5'(4'H)-oxazole], 2'-(1-methyl-1H-indol-3-yl)-, (-)-

128200-30-6
0 suppliers
inquiry

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Yield:-

Steps:

Multi-step reaction with 3 steps
1: (H3N)2HOP4, AcOH, PrNO2
2: 72 percent / methanol / 24 h / Ambient temperature
3: 66 percent / HCl / methanol / 1.) 12 h under reflux, 2.) 12 h reflux in saturated methanolic HCl

References:

Swain, Christopher J.;Kneen, Clare;Herbert, Richard;Baker, Raymond [Journal of the Chemical Society. Perkin transactions I,1990,# 11,p. 3183 - 3186]