Dodecylamine → HCID 89874072, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][C:19]=1[O:20][CH2:21][C:22]([F:25])([F:24])[F:23])[CH2:5][N:6]1C(=O)C2C(=CC=CC=2)C1=O.CCCCCCCCCCCCN>>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH2:5][NH2:6])[CH:17]=[CH:18][C:19]=1[O:20][CH2:21][C:22]([F:24])([F:25])[F:23]Participants
3
Procedure
The title compound is prepared in 89% yield (593 mg, an off-white solid) from 2-(3-chloro-4-(2,2,2-trifluoroethoxy)benzyl)isoindoline-1,3-dione (890 mg, 2.41 mmol, Step-2) in a similar manner to Step-5 of Amine-12.
Sources & evidence
- ORD record
- ord-2eef155ba1c84f67aba87cbe673147a5
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187475B2
Reaction notes
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