Hydrochloric Acid → HCID 53250879, compound
Reaction equation
[CH3:1][C:2]1([CH3:23])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]3[N:16]=[C:15]([N:17]4[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]4)[CH:14]=[CH:13][CH:12]=3)[CH:9]=2)[CH2:4][CH2:3]1.[OH:24][CH2:25][CH2:26][CH2:27][CH2:28][CH:29]=O.Cl>>[CH3:1][C:2]1([CH3:23])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]3[N:16]=[C:15]([N:17]4[CH2:22][CH2:21][N:20]([CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][OH:24])[CH2:19][CH2:18]4)[CH:14]=[CH:13][CH:12]=3)[CH:9]=2)[CH2:4][CH2:3]1Participants
4
Procedure
The preparation is carried out analogously to FS501 starting from 144 mg (0.47 mmol) of 1-[6-(3,3-dimethylindan-5-yl)pyridin-2-yl]piperazine and 96 mg (0.94 mmol) of 5-hydroxypentanal. The product is the hydrochloride.
Sources & evidence
- ORD record
- ord-9beaf10e34d0490f8a63bdf932de1aa0
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062015B2
Reaction notes
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