Hydrochloric Acid → HCID 67324274, compound
Reaction equation
Br.[CH3:2][CH:3]1[CH2:12][CH2:11][CH:10]([CH3:13])[C:9]2[CH:8]=[C:7]([C:14]3[N:15]=[C:16]([CH:19]4[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]4)[S:17][CH:18]=3)[CH:6]=[CH:5][C:4]1=2.[OH:25][CH2:26][CH2:27][CH2:28][CH2:29][CH:30]=O.Cl>>[CH3:2][CH:3]1[CH2:12][CH2:11][CH:10]([CH3:13])[C:9]2[CH:8]=[C:7]([C:14]3[N:15]=[C:16]([CH:19]4[CH2:24][CH2:23][N:22]([CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][OH:25])[CH2:21][CH2:20]4)[S:17][CH:18]=3)[CH:6]=[CH:5][C:4]1=2Participants
4
Procedure
The preparation was carried out as already described via a reductive amination starting from 100 mg (0.25 mmol) of 4-[4-(5,8-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)thiazol-2-yl]piperidine hydrobromide and 50 mg (0.49 mmol) of 5-hydroxypentanal. The product is in the form of the hydrochloride.
Sources & evidence
- ORD record
- ord-98e9edf460cb4a998f0b984975e43009
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08907098B2
Reaction notes
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