Diethylamine → HCID 18679561, compound

HRID 1633654Notes

Reaction equation

Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH:13]=[CH:12]2.[CH2:24]([NH:26][CH2:27][CH3:28])[CH3:25]>>[CH2:24]([N:26]([CH2:27][CH3:28])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH:13]=[CH:12]2)[CH3:25]

Participants

Reactant 2

HCID 8021Diethylamine

HCID 18679477HCID 18679477, compound

Product 1

HCID 18679561HCID 18679561, compound

Procedure

In analogy to example 4.4, 5-(6-Bromo-hexyloxy)-1-phenyl-1H-indole and diethylamine were converted to yield Diethyl-[6-(1-phenyl-1H-indol-5-yloxy)-hexyl]-amine as colorless oil, MS: 365 (MH+).

Sources & evidence

ORD record: ord-68be2ad3f76f474da073f83e9fe46ba0
Source dataset: uspto-grants-2003_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06503907B2

Reaction notes

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