4-(N-phthalimidomethylcarbonyl-N-methyl-amino)-aniline → HCID 178485775, compound

HRID 24852Notes

Reaction equation

HRID 24852 reaction equation
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=2)[NH:13][C:12]1=[O:23])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[C:24]1(=[O:46])[N:28]([CH2:29][C:30]([N:32]([C:34]2[CH:40]=[CH:39][C:37]([NH2:38])=[CH:36][CH:35]=2)[CH3:33])=[O:31])[C:27](=[O:41])[C:26]2=[CH:42][CH:43]=[CH:44][CH:45]=[C:25]12>CN(C=O)C>[C:27]1(=[O:41])[N:28]([CH2:29][C:30]([N:32]([C:34]2[CH:40]=[CH:39][C:37]([NH:38]/[C:4](=[C:11]3\[C:12](=[O:23])[NH:13][C:14]4[C:19]\3=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=4)/[C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=3)=[CH:36][CH:35]=2)[CH3:33])=[O:31])[C:24](=[O:46])[C:25]2=[CH:45][CH:44]=[CH:43][CH:42]=[C:26]12

Participants

4

Procedure

Prepared analogously to Example 89 from 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 4-(N-phthalimidomethylcarbonyl-N-methyl-amino)-aniline in DMF.

Sources & evidence

ORD record
ord-b61f44be29d949a6ba540ccc7115b29e
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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