HCID 86734407, compound → HCID 86734406, compound

HRID 1415100Notes

Reaction equation

HRID 1415100 reaction equation
[Cl:1]([O-:5])(=[O:4])(=[O:3])=[O:2].[CH2:6]([NH+:8]1[C:12]2=[N:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[N:20]=[C:11]2[N:10]2[CH2:21][CH2:22][CH:23]([CH3:31])[C:24]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[C:9]12)[CH3:7]>CS(C)=O>[Cl:1]([O-:5])(=[O:4])(=[O:3])=[O:2].[CH2:6]([NH+:8]1[C:12]2=[N:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[N:20]=[C:11]2[N:10]2[CH2:21][CH:22]=[C:23]([CH3:31])[C:24]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[C:9]12)[CH3:7]

Participants

3

Procedure

5-Ethyl-1,2-dihydro-3-methyl-4-phenyl-5H-pyrido[1',2':1,2]-imidazo[4,5-b]quinoxalinium perchlorate (3.1 g.) in 40 ml. of dimethyl sulfoxide is heated on a hot plate for 10 minutes. The dimethyl sulfoxide solution is poured into an excess of diethyl either and a green oil separates. The oil is crystallized from a chloroform-ether solution. Recrystallization from chloroform-ether affords 80% yield of product having a melting point of 262°-264° C.

Workup

  1. customThe oil is crystallized from a chloroform-ether solution
  2. customRecrystallization from chloroform-ether

Sources & evidence

ORD record
ord-c40866db9f8f42f2a577feab6b0cf4ee
Source dataset
uspto-grants-1977_01
Patent number
US04003750

Reaction notes

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