Hydrochloric Acid → HCID 67409413, compound
Reaction equation
[Br:1][C:2]1[C:3]([Cl:29])=[C:4]([C:8]2[O:9][C:10]3[C:15]([C:16](=[O:18])[CH:17]=2)=[C:14]([OH:19])[CH:13]=[C:12]([OH:20])[C:11]=3[C@@H:21]2[CH2:25][CH2:24][N:23]([CH3:26])[C@H:22]2[CH2:27][OH:28])[CH:5]=[CH:6][CH:7]=1.Cl>CO>[ClH:29].[Br:1][C:2]1[C:3]([Cl:29])=[C:4]([C:8]2[O:9][C:10]3[C:15]([C:16](=[O:18])[CH:17]=2)=[C:14]([OH:19])[CH:13]=[C:12]([OH:20])[C:11]=3[C@@H:21]2[CH2:25][CH2:24][N:23]([CH3:26])[C@H:22]2[CH2:27][OH:28])[CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound of example 29 (0.120 g, 0.24 mmol) was suspended in methanol (2 mL) and treated with ethereal HCl and the organic solvent was evaporated to afford the title salt.
Workup
- customthe organic solvent was evaporated
Sources & evidence
- ORD record
- ord-05ffe37bba62424ca3463ab6e2ad7e53
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906953B2
Reaction notes
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