2-(Ethylamino)ethanol → HCID 18679474, compound

HRID 1633655Notes

Reaction equation

HRID 1633655 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][CH2:28][OH:29])[CH3:25]>>[CH2:24]([N:26]([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)[CH2:27][CH2:28][OH:29])[CH3:25]

Participants

3

Reactant 2

HCID 80722-(Ethylamino)ethanolHCID 18679477HCID 18679477, compound

Product 1

HCID 18679474HCID 18679474, compound

Procedure

In analogy to example 4.4, 5-(6-Bromo-hexyloxy)-1-phenyl-1H-indole and 2-(ethylamino)ethanol were converted to yield 2-{Ethyl-[6-(1-phenyl-1H-indol-5-yloxy)-hexyl]-amino}-ethanol as colorless oil, MS: 381(MH+).

Sources & evidence

ORD record
ord-018064fe048e41d5824724cc520258c3
Source dataset
uspto-grants-2003_01
Patent number
US06503907B2

Reaction notes

Loading…