Hydrochloric Acid → HCID 18771795, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[S:8][CH:9]=[C:10]([NH:12][C:13](=[O:33])[NH:14][C:15]3[N:20]=[C:19]([CH2:21][N:22]4[CH2:27][CH2:26][CH:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:24][CH2:23]4)[CH:18]=[CH:17][CH:16]=3)[N:11]=2)=[CH:3][CH:2]=1.[ClH:34]>CO>[ClH:34].[N:1]1[CH:2]=[CH:3][C:4]([C:7]2[S:8][CH:9]=[C:10]([NH:12][C:13](=[O:33])[NH:14][C:15]3[N:20]=[C:19]([CH2:21][N:22]4[CH2:27][CH2:26][CH:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:24][CH2:23]4)[CH:18]=[CH:17][CH:16]=3)[N:11]=2)=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 1-{6-[3-(2-pyridin-4-yl-thiazol-4-yl)-ureido]-pyridin-2-ylmethyl}-piperidine-4-carboxylate (50 mg, 0.05 mmol, Example 61) in MeOH (5 mL) was treated with HCl (0.12 mL, 0.06 mmol, 1M in Et2O) to afford the title salt as a yellow solid.
Sources & evidence
- ORD record
- ord-04febf4cc3194296b6664cc5551f61ea
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645990B2
Reaction notes
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