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4-Hydroxy-7-[({5-hydroxy-7-[({3-[(4-methylphenyl)oxysulfonyl]phenyl}amino)sulfonyl](2-naphthyl)}amino)carbonylamino]naphthalene-2-sulfonic acid → HCID 9939539, compound

HRID 1791066
Notes
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Reaction equation

HRID 1791066 reaction equation
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([NH:12][C:13]([NH:15][C:16]3[CH:25]=[CH:24][C:23]4[C:18](=[CH:19][C:20]([S:27]([NH:30][C:31]5[CH:36]=[CH:35][CH:34]=[C:33]([S:37]([O:40]C6C=CC(C)=CC=6)(=[O:39])=[O:38])[CH:32]=5)(=[O:29])=[O:28])=[CH:21][C:22]=4[OH:26])[CH:17]=3)=[O:14])=[CH:9][CH:10]=2)[CH:5]=[C:4]([S:48]([OH:51])(=[O:50])=[O:49])[CH:3]=1.[Na+].[Na+].S(C1C=C(NS(C2C=C3C(C=CC(NC(NC4C=C5C(C=CC(S([O-])(=O)=O)=C5)=CC=4)=O)=C3)=CC=2)(=O)=O)C=CC=1)(O)(=O)=O.S(C1C=C(NS(C2C=C3C(C=CC(NC(NC4C=C5C(C=CC(S([O-])(=O)=O)=C5)=CC=4)=O)=C3)=CC=2)(=O)=O)C=CC=1)(O)(=O)=O>>[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([NH:12][C:13]([NH:15][C:16]3[CH:25]=[CH:24][C:23]4[C:18](=[CH:19][C:20]([S:27]([NH:30][C:31]5[CH:36]=[CH:35][CH:34]=[C:33]([S:37]([OH:40])(=[O:38])=[O:39])[CH:32]=5)(=[O:29])=[O:28])=[CH:21][C:22]=4[OH:26])[CH:17]=3)=[O:14])=[CH:9][CH:10]=2)[CH:5]=[C:4]([S:48]([OH:51])(=[O:50])=[O:49])[CH:3]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 98535304-Hydroxy-7-[({5-hydroxy-7-[({3-[(4-methylphenyl)oxysulfonyl]phenyl}amino)sulfonyl](2-naphthyl)}amino)carbonylamino]naphthalene-2-sulfonic acidHCID 131725845HCID 131725845, compound

Product 1

HCID 9939539HCID 9939539, compound

Procedure

This compound was prepared from compound 10 according to the procedure described for the synthesis of compound 12.

Sources & evidence

ORD record
ord-a9e74391cbf14242bd3b427717f72d39
Source dataset
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07071231B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes