Hydrogen Bromide → HCID 20058556, compound
Reaction equation
Cl.Cl.C[O:4][C:5]1[CH:6]=[C:7]([CH2:13][CH2:14][NH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][NH:22][CH2:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:8]=[CH:9][C:10]=1[O:11]C.[BrH:31]>>[BrH:31].[BrH:31].[C:25]1([CH2:24][CH2:23][NH:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][NH:15][CH2:14][CH2:13][C:7]2[CH:6]=[C:5]([OH:4])[C:10]([OH:11])=[CH:9][CH:8]=2)[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1Participants
3
Procedure
A solution of the diamine product of step (b) (4.75 g) in 48% aqueous hydrobromic acid (70 ml) was heated under reflux in an atmosphere of nitrogen for 3.5 hours. The solid which formed on cooling was filtered off and crystallised from ethanol, to give the title compound as the dihydrobromide salt, (3.1 g), mp 227°-228°.
Workup
- temperatureunder reflux in an atmosphere of nitrogen for 3.5 hours
- customThe solid which formed
- temperatureon cooling
- filtrationwas filtered off
- customcrystallised from ethanol
Sources & evidence
- ORD record
- ord-55ee93655cc54033b12d34a52a9abb1c
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04645768
Reaction notes
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