4-Carboxyphenylboronic Acid → Sodium (E)-2-((2Z,4E)-3-(4-carboxyphenyl)-5-(5-chloro-3,3-dimethyl-7-(3-sulfonatopropyl)-3H-pyrrolo[2,3-b]pyridin-7-ium-2-yl)penta-2,4-dienylidene)-3,3-dimethyl-1-(3-sulfonatopropyl)indoline-5-sulfonate
Reaction equation
C(CC[C:6]1[CH:7]=[C:8](/[C:12](/[CH:37]=[CH:38]/[C:39]2[C:40]([CH3:57])([CH3:56])[C:41]3[C:42]([N:55]=2)=[N+:43]([CH2:48][CH2:49][CH2:50][S:51]([O-:54])(=[O:53])=[O:52])[CH:44]=[C:45]([Cl:47])[CH:46]=3)=[CH:13]\[CH:14]=[C:15]2\[N:16]([CH2:30][CH2:31][CH2:32][S:33]([O-:36])(=[O:35])=[O:34])[C:17]3[C:22]([C:23]\2([CH3:25])[CH3:24])=[CH:21][C:20]([S:26]([O-:29])(=[O:28])=[O:27])=[CH:19][CH:18]=3)[CH:9]=[CH:10][CH:11]=1)(O)=O.[Na+:58].[Na+].[C:60](C1C=CC(B(O)O)=CC=1)([OH:62])=[O:61]>>[C:60]([C:11]1[CH:6]=[CH:7][C:8](/[C:12](/[CH:37]=[CH:38]/[C:39]2[C:40]([CH3:57])([CH3:56])[C:41]3[C:42]([N:55]=2)=[N+:43]([CH2:48][CH2:49][CH2:50][S:51]([O-:54])(=[O:52])=[O:53])[CH:44]=[C:45]([Cl:47])[CH:46]=3)=[CH:13]\[CH:14]=[C:15]2\[N:16]([CH2:30][CH2:31][CH2:32][S:33]([O-:36])(=[O:34])=[O:35])[C:17]3[C:22]([C:23]\2([CH3:25])[CH3:24])=[CH:21][C:20]([S:26]([O-:29])(=[O:28])=[O:27])=[CH:19][CH:18]=3)=[CH:9][CH:10]=1)([OH:62])=[O:61].[Na+:58].[Na+:58]Participants
3
Reactant 2
Product 1
Procedure
Compound 15 is prepared analogously to compound 10 (Example 10), except that 4-carboxyphenylboronic acid is used as a starting material. λMeOH=680 nm.
Sources & evidence
- ORD record
- ord-666f54776c754e209bd9b36228d22fc6
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927719B2
Reaction notes
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