HCID 15458808, compound → HCID 15513693, compound

HRID 1976727Notes

Reaction equation

HRID 1976727 reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[CH:9]=2)[C:4]([C:14](=O)[C:15](Cl)=[O:16])=[CH:3]1.Cl.C([O:23][C:24](=[NH:39])[CH2:25][C:26]1[C:34]2[C:29](=[C:30]([N+:35]([O-:37])=[O:36])[CH:31]=[CH:32][CH:33]=2)[N:28]([CH3:38])[CH:27]=1)(C)C>>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[CH:9]=2)[C:4]([C:14]2[C:15](=[O:16])[NH:39][C:24](=[O:23])[C:25]=2[C:26]2[C:34]3[C:29](=[C:30]([N+:35]([O-:37])=[O:36])[CH:31]=[CH:32][CH:33]=3)[N:28]([CH3:38])[CH:27]=2)=[CH:3]1

Participants

3

Reactant 2

HCID 15458808HCID 15458808, compoundHCID 70111988HCID 70111988, compound

Product 1

HCID 15513693HCID 15513693, compound

Procedure

ll) 3-(1-Methyl-6-nitro-1H-indol-3-yl)-4-(1-methyl-7-nitro-1H-indol-3-yl)-pyrrole-2,5-dione was prepared from (1-methyl-6-nitro-1H-indol-3-yl)-oxo-acetyl chloride and 2-(1-methyl-7-nitro-1H-indol-3-yl)-acetimidic acid isopropyl ester hydrochloride.

Sources & evidence

ORD record
ord-ecc0fbb1c36140818b0ad894979ae7b3
Source dataset
uspto-grants-2001_05
Patent number
US06228877B1

Reaction notes

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