Tetrahydrofuran → HCID 21962494, compound
Reaction equation
[CH:1]([N:14]1[C:22]2[C:17](=[CH:18][C:19]([Cl:23])=[CH:20][CH:21]=2)[C:16]([CH2:24][CH2:25][S:26]([C:29]2C=CC(C3C=C(C=CC=3)C(OC)=O)=[CH:31][CH:30]=2)(=[O:28])=[O:27])=[C:15]1[CH2:45][CH2:46][NH:47][S:48]([CH2:51][C:52]1[CH:57]=[CH:56][CH:55]=[CH:54][C:53]=1[Cl:58])(=[O:50])=[O:49])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:59]1[CH2:63][O:62][CH2:61][CH2:60]1.[OH-:64].[Na+]>CO>[CH:1]([N:14]1[C:22]2[C:17](=[CH:18][C:19]([Cl:23])=[CH:20][CH:21]=2)[C:16]([CH2:24][CH2:25][S:26]([C:29]2[CH:30]=[CH:31][C:60]([C:61]([OH:64])=[O:62])=[CH:59][CH:63]=2)(=[O:28])=[O:27])=[C:15]1[CH2:45][CH2:46][NH:47][S:48]([CH2:51][C:52]1[CH:57]=[CH:56][CH:55]=[CH:54][C:53]=1[Cl:58])(=[O:50])=[O:49])([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 3-[4-({2-[1-benzhydryl-5-chloro-2-(2-{[(2-chlorobenzyl)sulfonyl]amino}ethyl)-1H-indol-3-yl]ethyl}sulfonyl)phenyl]benzoate (1 eq), THF (0.1M), MeOH (1 mL/1 mL THF), and NaOH (1N) (11 eq) were stirred together overnight. Solvents were removed and the resulting residue was taken up in water. The solution was acidified with 1N HCl and collected resulting precipitate by filtration. Obtained 4-({2-[1-benzhydryl-5-chloro-2-(2-{[(2-chlorobenzyl)sulfonyl]amino}ethyl)-1H-indol-3-yl]ethyl}sulfonyl)benzoic acid (red-orange solid) in 80% yield. HRMS calc for [C39H34Cl2N2O6S2+H] 761.13081 found 761.13146.
Workup
- customSolvents were removed
- customcollected
- customresulting precipitate
- filtrationby filtration
Sources & evidence
- ORD record
- ord-06df637394ec40eeb808cac08ea36b67
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07713964B2
Reaction notes
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