6-ammonio-7-chloro-2,3(1H,4H)-quinoxalinedione chloride → 6-(2,5-Diphenyl-1-pyrrolyl)-7-chloro-2,3(1H,4H)-quinoxalinedione

HRID 1458809Notes

Reaction equation

HRID 1458809 reaction equation
[Cl-].[NH3+:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[Cl:13])[NH:9][C:8](=[O:14])[C:7](=[O:15])[NH:6]2.[C:16]1([C:22]2(OC)[CH2:26][CH2:25][C:24]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)(OC)O2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[C:16]1([C:22]2[N:2]([C:3]3[CH:4]=[C:5]4[C:10](=[CH:11][C:12]=3[Cl:13])[NH:9][C:8](=[O:14])[C:7](=[O:15])[NH:6]4)[C:24]([C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Participants

3

Reactant 2

HCID 220971776-ammonio-7-chloro-2,3(1H,4H)-quinoxalinedione chlorideHCID 220972192,5-Diphenyl-2,5-dimethoxytetrahydrofuran

Product 1

HCID 220971726-(2,5-Diphenyl-1-pyrrolyl)-7-chloro-2,3(1H,4H)-quinoxalinedione

Procedure

16.5 mmol of 6-ammonio-7-chloro-2,3(1H,4H)-quinoxalinedione chloride were reacted with 16.5 mmol of 2,5-diphenyl-2,5-dimethoxytetrahydrofuran by the method of Example 5d.

Sources & evidence

ORD record
ord-ea1eef2f42014125a16430b8504efe3b
Source dataset
uspto-grants-1998_12
Patent number
US05852017

Reaction notes

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