Reaktion #95132

ord-41f04a67a76e43fbbe602296aada1648

Reaktionsgleichung

Cc1[nH]c2ccc(O)cc2c1-c1ccncc1
2-methyl-3-(4-pyridyl)-1H-indole-5-ol
CCOC(=O)C(C)(C)Br
2-bromo-2-methyl-propanoic acid ethylester
→
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3ccncc3)c2c1
2-Methyl-2-[2-methyl-3-(4-pyridyl)-1H-indole-5-yloxy]-propanoic acid ethylester

Edukte

Cc1[nH]c2ccc(O)cc2c1-c1ccncc1
2-methyl-3-(4-pyridyl)-1H-indole-5-ol
CCOC(=O)C(C)(C)Br
2-bromo-2-methyl-propanoic acid ethylester

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The above compound was prepared from 2-methyl-3-(4-pyridyl)-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester using a procedure analogous to that of Example 10.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04343811uspto-grants-1982_08