Ethyl Bromide → 3-ethyl-1H-indol-6-amine

HRID 2404659Notes

Reaction equation

HRID 2404659 reaction equation
[N+:1]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[CH:9][NH:10]2)=[CH:6][CH:5]=1)([O-])=O.[CH2:13](Br)[CH3:14]>CC#N>[CH2:13]([C:8]1[C:7]2[C:11](=[CH:12][C:4]([NH2:1])=[CH:5][CH:6]=2)[NH:10][CH:9]=1)[CH3:14]

Participants

4

Procedure

3-Ethyl-1H-indol-6-ylamine (B-12) was synthesized following the general scheme above starting from 6-nitroindole and ethyl bromide. Overall yield (42%). HPLC ret. time 1.95 min, 10-99% CH3CN, 5 min run; ESI-MS 161.3 m/z (MH+).

Workup

  1. customOverall yield (42%)

Sources & evidence

ORD record
ord-cbf0ef0a72e245509014582e9bc2af85
Source dataset
uspto-grants-2014_08
Patent number
US08802700B2

Reaction notes

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