Reaktion #95134

ord-8e7bd4c2217c4f9780c50df7315bb7cb

Reaktionsgleichung

Oc1ccc2[nH]c(Cc3ccccc3)c(-c3ccncc3)c2c1
2-benzyl-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(Cc3ccccc3)c(-c3ccncc3)c2c1
2-[2-Benzyl-3-(4-pyridyl)-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester

Edukte

Oc1ccc2[nH]c(Cc3ccccc3)c(-c3ccncc3)c2c1
2-benzyl-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-benzyl-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