Hydrochloric Acid → HCID 69817674, compound
Reaction equation
[ClH:1].[OH:2][CH2:3][C@@H:4]([NH:22][CH2:23][C@H:24]([OH:33])[CH2:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13]([NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:14])=[CH:8][CH:7]=1>CO>[ClH:1].[OH:2][CH2:3][C@@H:4]([NH:22][CH2:23][C@H:24]([OH:33])[CH2:25][O:26][C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13]([NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:14])=[CH:8][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 10% hydrogen chloride in methanol was added N-[4-[(2S)-3-hydroxy-2-[[(2S)-2-hydroxy-3-phenoxypropyl]amino)propyl]phenyl]-N′-phenylurea (70 mg) and stirred for 15 minutes. The reaction mixture was concentrated and followed by recrystallization from ethanol to give N-[4-[(2S)-3-hydroxy-2-([(2S)-2-hydroxy-3-phenoxypropyl]amino]propyl]phenyl]-N′-phenylurea hydrochloride (38 mg) as a white powder.
Workup
- concentrationThe reaction mixture was concentrated
- customfollowed by recrystallization from ethanol
Sources & evidence
- ORD record
- ord-8c893b9eca7e476abcfcfae418edf41d
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06826033B2
Reaction notes
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