Acetic Acid → HCID 69043488, compound

HRID 1841274Notes

Reaction equation

HRID 1841274 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2.[CH:12]([O:19][CH2:20][CH3:21])([O:16]CC)OCC.[N+:22]([CH2:25][C:26](OCC)=O)([O-])=O.[C:31](O)(=O)C>[Fe]>[CH2:20]([O:19][C:12]([C:25]1[N:22]=[CH:31][N:1]([C:2]2[CH:3]=[CH:4][CH:5]=[C:6]3[C:11]=2[N:10]=[CH:9][CH:8]=[CH:7]3)[CH:26]=1)=[O:16])[CH3:21]

Participants

6

Procedure

Following the general method described in example 384, 8-aminoquinoline was reacted with triethyl orthoformate, ethyl nitroacetate and acetic acid followed by treatment with triethyl orthoformate, iron and acetic acid. After workup and chromatography the title compound was obtained as a light brown crystalline solid. Mp. >92° C. dec. (AcOEt/hexane), MS: m/e=267 (M+).

Sources & evidence

ORD record
ord-ec3a2dca9b51457d8d8b4ed0c924cc6b
Source dataset
uspto-grants-2004_01
Patent number
US06683097B2

Reaction notes

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