2-(Ethylamino)ethanol → HCID 89906420, compound
Reaction equation
[Br:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[C:6]([CH:21]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][C:17]([F:20])([F:19])[F:18])=[CH:12][CH:11]=1)=[O:8].[CH2:23]([NH:25][CH2:26][CH2:27][OH:28])[CH3:24]>>[Br:1][C:2]1[C:3]([N:25]([CH2:23][CH3:24])[CH2:26][CH2:27][OH:28])=[N:4][CH:5]=[C:6]([CH:21]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][C:17]([F:20])([F:19])[F:18])=[CH:12][CH:11]=1)=[O:8]Participants
3
Procedure
The title compound was prepared in an analogous fashion to that described in Stage 33.1 using 5-bromo-6-chloro-N-(4-((trifluoromethyl)thio)phenyl)nicotinamide (Stage 185.2) and 2-ethylamino-ethanol to afford a white crystalline solid. (Reaction Time was 10 h). HPLC (Condition 4) tR=6.33 min, UPLC-MS (Condition 3) tR=1.25 min, m/z=466.2 [M+H]+.
Workup
- customto afford a white crystalline solid
- custom(Reaction Time was 10 h)
Sources & evidence
- ORD record
- ord-bd2e7cc521f446db80c1114e33895e39
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09278981B2
Reaction notes
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