Sodium Hydroxide → HCID 11699853, compound
Reaction equation
Cl.Cl.[CH:3]1([O:9][C:10]2[CH:11]=[C:12]([C:26]3[CH:31]=[CH:30][C:29]([CH2:32][CH2:33][NH:34][CH2:35][C@H:36]([OH:43])[C:37]4[CH:38]=[N:39][CH:40]=[CH:41][CH:42]=4)=[CH:28][CH:27]=3)[CH:13]=[CH:14][C:15]=2[C:16]([NH:18][S:19]([CH2:22][CH2:23][CH2:24][OH:25])(=[O:21])=[O:20])=[O:17])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.[OH-].[Na+]>O>[CH:3]1([O:9][C:10]2[CH:11]=[C:12]([C:26]3[CH:27]=[CH:28][C:29]([CH2:32][CH2:33][NH:34][CH2:35][C@H:36]([OH:43])[C:37]4[CH:38]=[N:39][CH:40]=[CH:41][CH:42]=4)=[CH:30][CH:31]=3)[CH:13]=[CH:14][C:15]=2[C:16]([NH:18][S:19]([CH2:22][CH2:23][CH2:24][OH:25])(=[O:20])=[O:21])=[O:17])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3-(cyclohexyloxy)-N-[(3-hydroxypropyl)sulfonyl]-4′-[2-[[(2R)-2-hydroxy-2-(3-pyridyl)ethyl]amino]ethyl]-4-biphenylcarboxamide dihydrochloride (1.2 g) in water (5 ml) was added 1N sodium hydroxide aqueous solution (3.7 ml). The obtained solid was filtrated and then followed by crystallization from isopropyl alcohol to give 3-(cyclohexyloxy)-N-[(3-hydroxypropyl)sulfonyl]-4′-[2-[[(2R)-2-hydroxy-2-(3-pyridyl)ethyl]amino]ethyl]-4-biphenylcarboxamide (1.0 g).
Workup
- filtrationThe obtained solid was filtrated
- customfollowed by crystallization from isopropyl alcohol
Sources & evidence
- ORD record
- ord-5cc2fcbbf5044a9e8cdc35aba71d8d1f
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07928264B2
Reaction notes
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