HCID 23146084, compound → 1-(4-(2-(Dimethylamino)ethoxy)phenyl)butan-1-amine
Reaction equation
[CH2:1]([N:3]([CH2:18]C)[CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]([NH2:17])[CH2:14][CH2:15][CH3:16])=[CH:9][CH:8]=1)C.CN(C)CCOC1C=CC(C(=O)CCC)=CC=1>>[CH3:18][N:3]([CH3:1])[CH2:4][CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([CH:13]([NH2:17])[CH2:14][CH2:15][CH3:16])=[CH:11][CH:12]=1Participants
3
Procedure
The title compound was prepared by using a similar procedure as described for the preparation of 25 except that 1-(4-(2-(dimethylamino)ethoxy)phenyl)butan-1-one (22) was used instead of 1-(4-(2-(diethylamino)ethoxy)phenyl)butan-1-one (21). This produced crude 26 (410 mg, 73%) as a yellow oil: MS (ES+) m/z 237.1 (M+H)+.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-efba2276936e4dbeba0c17a0186321ed
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809377B2
Reaction notes
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