ethyl 5-fluoro-1H-indole-2-carboxylate → ethyl 5-fluoro-1-[2-[(5-methylpyridin-2-yl)oxy]-ethyl]-1H-indole-2-carboxylate

HRID 2063285Notes

Reaction equation

HRID 2063285 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:5]2.[CH3:16][C:17]1[CH:18]=[CH:19][C:20]([O:23][CH2:24][CH2:25]O)=[N:21][CH:22]=1>>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:25][CH2:24][O:23][C:20]1[CH:19]=[CH:18][C:17]([CH3:16])=[CH:22][N:21]=1)[C:6]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:5]2

Participants

3

Reactant 2

HCID 2727899ethyl 5-fluoro-1H-indole-2-carboxylateHCID 207951692-[(5-Methylpyridin-2-yl)oxy]ethanol

Product 1

HCID 66811445ethyl 5-fluoro-1-[2-[(5-methylpyridin-2-yl)oxy]-ethyl]-1H-indole-2-carboxylate

Procedure

The ethyl 5-fluoro-1-[2-[(5-methylpyridin-2-yl)oxy]-ethyl]-1H-indole-2-carboxylate intermediate is prepared in a manner similar to the method described in Example 18.1, from ethyl 5-fluoro-1H-indole-2-carboxylate and 2-(5-methylpyridin-2-yloxy)ethanol prepared in the preceding step.

Workup

  1. customprepared in the preceding step

Sources & evidence

ORD record
ord-5e9187a751514a87ba6de4223fccfdd5
Source dataset
uspto-grants-2012_10
Patent number
US08288376B2

Reaction notes

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