Hydrochloric Acid → HCID 18771691, compound
Reaction equation
[ClH:1].[Br:2][C:3]1[S:7][C:6]([C:8]2[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=2)=[N:5][C:4]=1[NH:14][C:15]([NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24][N:25]([CH2:28][CH3:29])[CH2:26][CH3:27])[N:19]=1)=[O:16].CO>CCOCC>[ClH:1].[Br:2][C:3]1[S:7][C:6]([C:8]2[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=2)=[N:5][C:4]=1[NH:14][C:15]([NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24][N:25]([CH2:28][CH3:29])[CH2:26][CH3:27])[N:19]=1)=[O:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
HCl (54 μL, 0.054 mmol, 1.0 M soln in Et2O) was added to 1-[5-bromo-2-(pyridin-4-yl)thiazol-4-yl)-3-(6-diethylaminomethyl-pyridin-2-yl)urea (25 mg, 0.054 mmol, Example 180) in a solution of MeOH (0.5 mL) to give a yellow solid.
Workup
- customto give a yellow solid
Sources & evidence
- ORD record
- ord-57a26b4a4cad40f1b7b31795546d8b71
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196104B2
Reaction notes
Loading…