Dodecylamine → HCID 89874838, compound
Reaction equation
[CH3:1][C:2]1[C:7]([O:8][CH2:9][CH2:10][C:11]([F:14])([F:13])[F:12])=[CH:6][N:5]=[C:4]([CH2:15][N:16]2C(=O)C3C(=CC=CC=3)C2=O)[CH:3]=1.CCCCCCCCCCCCN>>[CH3:1][C:2]1[C:7]([O:8][CH2:9][CH2:10][C:11]([F:14])([F:12])[F:13])=[CH:6][N:5]=[C:4]([CH2:15][NH2:16])[CH:3]=1Participants
3
Procedure
The title compound is prepared in 69% yield (133 mg, a pale brown oil) from 2-((4-methyl-5-(3,3,3-trifluoropropoxy)pyridin-2-yl)methyl)isoindoline-1,3-dione (300 mg, 0.82 mmol, Step-4) in a similar manner to Step-5 of Amine-12.
Sources & evidence
- ORD record
- ord-ddd7653dbecc43d7837d1fbba198c22c
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187475B2
Reaction notes
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