Hydrochloric Acid → HCID 18772033, compound
Reaction equation
[ClH:1].[N:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][CH:10]=[C:11]([NH:13][C:14](=[O:34])[NH:15][C:16]3[N:21]=[C:20]([CH2:22][N:23]4[CH2:28][CH2:27][CH2:26][CH2:25][CH:24]4[C:29]([O:31][CH2:32][CH3:33])=[O:30])[CH:19]=[CH:18][CH:17]=3)[N:12]=2)=[CH:4][CH:3]=1.CO>CCOCC>[ClH:1].[N:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:9][CH:10]=[C:11]([NH:13][C:14](=[O:34])[NH:15][C:16]3[N:21]=[C:20]([CH2:22][N:23]4[CH2:28][CH2:27][CH2:26][CH2:25][CH:24]4[C:29]([O:31][CH2:32][CH3:33])=[O:30])[CH:19]=[CH:18][CH:17]=3)[N:12]=2)=[CH:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
HCl (0.12 mL, 0.12 mmol, 1.0 M soln in Et2O) was added to ethyl 1-[6-[3-(2-(pyridin-4-yl)thiazol-4-yl)ureido]-pyridin-2-ylmethyl]piperidine-2-carboxylate (50 mg, 0.11 mmol, Example 74) in a solution of MeOH (2 mL) to give a pale yellow solid.
Workup
- customto give a pale yellow solid
Sources & evidence
- ORD record
- ord-7d3f9ede9b234944a1bf40d5d22cbc0b
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645990B2
Reaction notes
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