4,7-Dichloroquinoline → HCID 131715826, compound

HRID 2292262Notes

Reaction equation

HRID 2292262 reaction equation
O[N:2]1[C:6](=[O:7])[C:5]2=[CH:8][CH:9]=[CH:10][CH:11]=[C:4]2[C:3]1=[O:12].Cl[C:14]1[C:23]2[C:18](=[CH:19][C:20]([Cl:24])=[CH:21][CH:22]=2)[N:17]=[CH:16][CH:15]=1>>[Cl:24][C:20]1[CH:19]=[C:18]2[C:23]([C:14]([C:5]34[CH:8]=[CH:9][CH:10]=[CH:11][CH:4]3[C:3]([NH:2][C:6]4=[O:7])=[O:12])=[CH:15][CH:16]=[N:17]2)=[CH:22][CH:21]=1

Participants

3

Reactant 2

HCID 68664,7-DichloroquinolineHCID 10665N-Hydroxyphthalimide

Product 1

HCID 131715826HCID 131715826, compound

Procedure

N-hydroxy-phthalimide and 4,7-dichloro-quinoline were reacted to form 0-(7-chloro-4-quinolyl)-phthalimide melting at 225° C. and the latter is reacted to obtain 0-(7-chloro-4- quinolyl)-hydroxylamine melting at 175° C.

Sources & evidence

ORD record
ord-76b002e2d6f94572b97508ec7cc43ea2
Source dataset
uspto-grants-1989_01
Patent number
US04801717

Reaction notes

Loading…