HCID 21290002, compound → HCID 15005594, compound

HRID 867497Notes

Reaction equation

HRID 867497 reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:11][CH2:12][CH2:13][O:14][C:15]2[CH:24]=[CH:23][C:22]3[N:21]=[C:20]4[NH:25][C:26](=[O:28])[NH:27][C:19]4=[CH:18][C:17]=3[CH:16]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[N+](C1C=CC(OCCCS(C2C=CC(Cl)=CC=2)(=O)=O)=CC=1C=C1NC(=O)NC1=O)([O-])=O>>[C:5]1([S:8]([CH2:11][CH2:12][CH2:13][O:14][C:15]2[CH:24]=[CH:23][C:22]3[N:21]=[C:20]4[NH:25][C:26](=[O:28])[NH:27][C:19]4=[CH:18][C:17]=3[CH:16]=2)(=[O:10])=[O:9])[CH:4]=[CH:3][CH:2]=[CH:7][CH:6]=1

Participants

3

Reactant 2

HCID 21290002HCID 21290002, compoundHCID 54528584HCID 54528584, compound

Product 1

HCID 15005594HCID 15005594, compound

Procedure

1,3-Dihydro-7-[3-[(4-chlorophenyl)sulfonyl]propoxy]-2H-imidazo[4,5-b]quinolin-2-one was analogously prepared from 5-[[2-nitro-5-[3-[(4-chlorophenyl)sulfonyl]propoxy]phenyl]methylene]-2,4-imidazolidinedione.

Sources & evidence

ORD record
ord-d6dea7710fc24cc5829515995561e1ff
Source dataset
uspto-grants-1988_10
Patent number
US04775674

Reaction notes

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