Hydrochloric Acid → HCID 69410895, compound
Reaction equation
[ClH:1].[N:2]1([CH2:9][C:10]2[N:15]=[C:14]([NH:16][C:17]([NH:19][C:20]3[N:21]=[C:22]([C:25]4[CH:30]=[CH:29][N:28]=[CH:27][CH:26]=4)[S:23][CH:24]=3)=[O:18])[CH:13]=[CH:12][CH:11]=2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.CO>CCOCC>[ClH:1].[N:2]1([CH2:9][C:10]2[N:15]=[C:14]([NH:16][C:17]([NH:19][C:20]3[N:21]=[C:22]([C:25]4[CH:30]=[CH:29][N:28]=[CH:27][CH:26]=4)[S:23][CH:24]=3)=[O:18])[CH:13]=[CH:12][CH:11]=2)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
HCl (0.29 mL, 0.28 mmol, 1.0 M soln in Et2O) was added to 1-(6-azepan-1-ylmethyl-pyridin-2-yl)-3-(2-pyridin-4-yl-thiazol-4-yl)urea (106 mg, 0.26 mmol, Example 71) in a solution of MeOH (4 mL) and the resulting mixture stirred 6 h. Concentration in vacuo gave a yellow solid.
Workup
- concentrationConcentration in vacuo
- customgave a yellow solid
Sources & evidence
- ORD record
- ord-0fdec9977db0413ea47885b12f8b0d6a
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196104B2
Reaction notes
Loading…