(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole

CAS No.
15266-46-3
Chemical Name:
(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole
Synonyms
Aids003034;Aids-003034;Voaphylline;Conoflorine;(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole;2H-3,13-Methanooxireno[9,10]azacycloundecino[5,4-B]indole, 13-ethyl-1A,4,5,10,11,12,13,13A-octahydro-, (1ar,13S,13as)-
CBNumber:
CB22286154
Molecular Formula:
C19H24N2O
Molecular Weight:
296.41
MDL Number:
MOL File:
15266-46-3.mol

(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole Properties

Melting point 164-6°C

(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole Chemical Properties,Uses,Production

Description

The alkaloidal extract from the dried leaves of Voacanga africana, after chromatographic separation, yield this indole alkaloid which is purified by recrystallization from MeOH when it forms colourless needles. It has [α]578 + 28° (CHCI3) and gives an ultraviolet spectrum in EtOH with absorption maxima at 230, 285 and 290 mμ.

References

Kunesch, Das, Poisson., Bull. Soc., Chim. Fr., 2155 (1967)

(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole Preparation Products And Raw materials

Raw materials

Preparation Products

(1aR,13S,13aS)-13-Ethyl-1a,4,5,10,11,12,13,13a-octahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indole Conoflorine Voaphylline 2H-3,13-Methanooxireno[9,10]azacycloundecino[5,4-B]indole, 13-ethyl-1A,4,5,10,11,12,13,13A-octahydro-, (1ar,13S,13as)- Aids003034 Aids-003034 15266-46-3