Dodecylamine → HCID 89874685, compound
Reaction equation
[F:1][C:2]([F:25])([CH3:24])[CH2:3][O:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][N:12]2C(=O)C3C(=CC=CC=3)C2=O)=[CH:7][C:6]=1[CH3:23].CCCCCCCCCCCCN>>[F:25][C:2]([F:1])([CH3:24])[CH2:3][O:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][NH2:12])=[CH:7][C:6]=1[CH3:23]Participants
3
Procedure
The title compound is prepared in 95% yield (699 mg, colorless oil) from 2-((6-(2,2-difluoropropoxy)-5-methylpyridin-3-yl)methyl)isoindoline-1,3-dione (1.18 g, 3.41 mmol) in a similar manner to Step-5 of Amine-12.
Sources & evidence
- ORD record
- ord-649d4235ae184421be03cf40b33614a9
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187475B2
Reaction notes
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