Water → HCID 54013770, compound

HRID 1419888Notes

Reaction equation

HRID 1419888 reaction equation
[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[O:23][CH3:24])=[CH:13][CH:12]=[CH:11][C:10]=2[O:25][CH2:26][CH2:27][CH2:28][S:29][CH3:30])(=[O:5])[CH2:2][CH2:3][CH3:4].[OH2:31].[O-]Cl.[Na+]>C(Cl)Cl>[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[O:23][CH3:24])=[CH:13][CH:12]=[CH:11][C:10]=2[O:25][CH2:26][CH2:27][CH2:28][S:29]([CH3:30])=[O:31])(=[O:5])[CH2:2][CH2:3][CH3:4]

Participants

5

Reactant 3

HCID 962WaterHCID 23665760Sodium HypochloriteHCID 53756819HCID 53756819, compound

Product 1

HCID 54013770HCID 54013770, compoundYield 4.6%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

3-butyryl-4-(2-methoxyphenylamino)-8-(3-methylthiopropoxy)quinoline (0.30 g, 0.70 mmol) was dissolved in methylene chloride (10 ml), 5 ml water was added and then a solution of 1.5 ml (1.09 mmol) of 5% NaOCl in 10 ml methylene chloride was added. The mixture was stirred for 4 h at room temperature. The organic phase was separated and evaporated. Chromatography with methylene chloride methanol 95:5 as the eluent gave 14 mg (4.6%) of the title compound.

Workup

  1. customThe organic phase was separated
  2. customevaporated

Sources & evidence

ORD record
ord-7a9143d7acc241fea09aeaab453192e8
Source dataset
uspto-grants-1999_03
Patent number
US05889021

Reaction notes

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