Reaktion #42649

ord-df96e00f5e93401da2e695082925d9be

Reaktionsgleichung

Cn1ccc2ccccc21
N-methyl indole
CS(=O)(=O)O.O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
P2O5 MeSO3H
[N].c1ccc2[nH]ccc2c1
indole nitrogen
CI
MeI
c1ccc2[nH]ccc2c1
esters
c1ccc2[nH]ccc2c1
indole
O=C([O-])[O-].[K+].[K+]
K2CO3
→
O=C1CCNC(=O)c2[nH]ccc21
aldisine

Edukte

Cn1ccc2ccccc21
N-methyl indole
CS(=O)(=O)O.O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
P2O5 MeSO3H
[N].c1ccc2[nH]ccc2c1
indole nitrogen
CI
MeI
c1ccc2[nH]ccc2c1
esters
c1ccc2[nH]ccc2c1
indole
O=C([O-])[O-].[K+].[K+]
K2CO3

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas used for the synthesis of 3

Vorschrift

Starting with the commercially available 2-indolecarboxylic acid, condensation with the ethyl ester of β-alanine in the presence of EDCI and DMAP, provided the indole 4. Methylation of the indole nitrogen with MeI and K2CO3 proceeded in near quantitative yields, rendering the N-methyl indole, which was used for the synthesis of 3. Hydrolysis of esters 4 and 5 followed by the P2O5/MeSO3H mediated cyclization provided the key intermediate aldisine derivatives 8 and 9.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732436B2uspto-grants-2010_06