Sodium Hydroxide → HCID 178494500, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=[C:13](Cl)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]1=[O:21])(=O)C.Cl.[CH3:23][O:24][CH2:25][C:26]1[CH:27]=[C:28]([CH:30]=[CH:31][CH:32]=1)[NH2:29].[OH-].[Na+]>C1COCC1.CO>[CH3:23][O:24][CH2:25][C:26]1[CH:27]=[C:28]([NH:29]/[C:13](=[C:6]2\[C:5](=[O:21])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[CH:10][CH:11]=3)/[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:30]=[CH:31][CH:32]=1Participants
6
Procedure
Prepared analogously to Example 2 from 1-acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone and 3-methoxymethyl-aniline-hydrochloride in THF and subsequent treatment with sodium hydroxide solution in methanol.
Sources & evidence
- ORD record
- ord-48b6d2d452b74375a4e06cb6cdb23a9b
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855710B2
Reaction notes
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