Tetrahydrofuran → HCID 21962494, compound

HRID 2237104Notes

Reaction equation

HRID 2237104 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]=1

Participants

5

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

  1. customSolvents were removed
  2. customcollected
  3. customresulting precipitate
  4. filtrationby filtration

Sources & evidence

ORD record
ord-06df637394ec40eeb808cac08ea36b67
Source dataset
uspto-grants-2010_05
Patent number
US07713964B2

Reaction notes

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