Ammonia → HCID 178517278, compound

HRID 24800

Reaction equation

HRID 24800 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=2)[C:6](=[C:16](OC)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:5]1=[O:25])(=O)C.[O:26]1[CH2:31][CH2:30][N:29]([C:32]2[CH:38]=[CH:37][C:35]([NH2:36])=[CH:34][CH:33]=2)[CH2:28][CH2:27]1.N>ClCCl>[O:26]1[CH2:27][CH2:28][N:29]([C:32]2[CH:38]=[CH:37][C:35]([NH:36]/[C:16](=[C:6]3\[C:5](=[O:25])[NH:4][C:12]4[C:7]\3=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=4)/[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)=[CH:34][CH:33]=2)[CH2:30][CH2:31]1

Participants

5

Procedure

Prepared analogously to Example 77 from 1-acetyl-3-(1-methoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 4-morpholinoaniline in dichloromethane and subsequent treatment with methanolic ammonia.

Sources & evidence

ORD record
ord-3d9852db331a4c56a82063a7cc1d760e
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Linked notes

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