Allyl Alcohol → HCID 59168169, compound

HRID 1444064Notes

Reaction equation

HRID 1444064 reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[S:9]([NH:12][C:13]1[C:18](Cl)=[N:17][C:16]([Cl:20])=[CH:15][N:14]=1)(=[O:11])=[O:10].[CH2:21]([OH:24])[CH:22]=[CH2:23]>>[CH2:21]([O:24][C:18]1[C:13]([NH:12][S:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([Cl:8])[C:2]=2[Cl:1])(=[O:11])=[O:10])=[N:14][CH:15]=[C:16]([Cl:20])[N:17]=1)[CH:22]=[CH2:23]

Participants

3

Reactant 2

HCID 7858Allyl AlcoholHCID 101263402,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide

Product 1

HCID 59168169HCID 59168169, compound

Procedure

Prepared by the method of Example 31 using allyl alcohol (10 mL) as solvent and 2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide (Example 74) (0.35 g). Yield 0.32 g.

Sources & evidence

ORD record
ord-554618a7683a4ae286de8a7f69638a30
Source dataset
uspto-grants-2010_02
Patent number
US07662825B2

Reaction notes

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