Hydrochloric Acid → HCID 70344612, compound
Reaction equation
[CH2:1]([N:3]1[CH:7]=[C:6]([CH:8]=[CH:9][C:10]2[S:11][C:12]3[NH:13][CH2:14][CH2:15][CH2:16][C:17]=3[N:18]=2)[N:5]=[C:4]1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:2].[ClH:25]>>[ClH:25].[ClH:25].[CH2:1]([N:3]1[CH:7]=[C:6]([CH:8]=[CH:9][C:10]2[S:11][C:12]3[NH:13][CH2:14][CH2:15][CH2:16][C:17]=3[N:18]=2)[N:5]=[C:4]1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:2]Participants
3
Procedure
2-{2-(1-Ethyl-2-phenylimidazol-4-yl)ethenyl}-4,5,6,7-tetrahydrothiazolo[5,4-b]pyridine was neutralized with hydrochloric acid and recrystallized from ethanoldiethyl ether to obtain the title compound (yield: 94.2%).
Workup
- customrecrystallized from ethanoldiethyl ether
Sources & evidence
- ORD record
- ord-7ea6ee1f157644adbcc03fcd488e5731
- Source dataset
- uspto-grants-1992_10
- Patent number
- US05153201
Reaction notes
Loading…