Hydrogen Bromide → HCID 69058106, compound
Reaction equation
[N:1]1([C:7]([O:9][C@H:10]([CH2:37][C:38]2[CH:43]=[C:42]([CH3:44])[C:41]([OH:45])=[C:40]([CH3:46])[CH:39]=2)[C:11]([N:13]2[CH2:18][CH2:17][C:16]([N:25]3[CH2:31][CH2:30][C:29]4[CH:32]=[CH:33][CH:34]=[CH:35][C:28]=4[NH:27][C:26]3=[O:36])([N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[CH2:15][CH2:14]2)=[O:12])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[BrH:47]>C(O)CC>[BrH:47].[N:1]1([C:7]([O:9][C@H:10]([CH2:37][C:38]2[CH:43]=[C:42]([CH3:44])[C:41]([OH:45])=[C:40]([CH3:46])[CH:39]=2)[C:11]([N:13]2[CH2:14][CH2:15][C:16]([N:25]3[CH2:31][CH2:30][C:29]4[CH:32]=[CH:33][CH:34]=[CH:35][C:28]=4[NH:27][C:26]3=[O:36])([N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[CH2:17][CH2:18]2)=[O:12])=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
0.5 g (0.79 mmol) 4-(1,2,4,5-tetrahydro-2-oxo-3H-1,3-benzodiazepin-3-yl)-(1R)-1-[(4-hydroxy-3,5-dimethylphenyl)methyl]-2-[4-(4-morpholinyl)-1-piperidinyl]-2-oxoethyl 1-piperidinecarboxylate are suspended in 5 ml n-propanol at ambient temperature and heated to 70° C. After the addition of 157 μl hydrobromic acid (30% in glacial acetic acid) the mixture is stirred for 1 hour at 70° C. and 20 hours at 40° C. Then the suspension formed is cooled to ambient temperature, stirred for 5 hours and filtered. The residue is dried for 4 hours at 80° C.
Workup
- customThen the suspension formed
- temperatureis cooled to ambient temperature
- stirringstirred for 5 hours
- filtrationfiltered
- customThe residue is dried for 4 hours at 80° C.
Sources & evidence
- ORD record
- ord-80aa1b2170ed4943a2a7df02c37832d1
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07638625B2
Reaction notes
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