Ethanolamine → HCID 77231000, compound
Reaction equation
[Br:1][C:2]1[N:7]=[C:6]([N:8]2[CH2:14][CH2:13][CH2:12][CH:11]([NH:15][CH2:16][CH2:17]CCO)[CH2:10][CH2:9]2)[CH:5]=[CH:4][CH:3]=1.C(CN)[OH:22]>>[Br:1][C:2]1[N:7]=[C:6]([N:8]2[CH2:14][CH2:13][CH2:12][CH:11]([NH:15][CH2:16][CH2:17][OH:22])[CH2:10][CH2:9]2)[CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
The preparation is carried out analogously to 4-[1-(6-bromopyridin-2-yl)azepan-4-ylamino]butan-1-ol starting from 99 μl (1.65 mmol) of ethanolamine 85 mg, colourless oil, Rt.=1.55 min (method B), LCMS: 315 (M+H).
Workup
- custom=1.55 min (method B), LCMS
Sources & evidence
- ORD record
- ord-e86824a266174351bc70f19e640a72ce
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062015B2
Reaction notes
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