Propargyl alcohol → HCID 59168181, compound

HRID 1444065Notes

Reaction equation

HRID 1444065 reaction equation
[CH2:1]([OH:4])[C:2]#[CH:3].[Cl:5][C:6]1[C:11]([Cl:12])=[CH:10][CH:9]=[CH:8][C:7]=1[S:13]([NH:16][C:17]1[C:22](Cl)=[N:21][C:20]([Cl:24])=[CH:19][N:18]=1)(=[O:15])=[O:14]>>[Cl:5][C:6]1[C:11]([Cl:12])=[CH:10][CH:9]=[CH:8][C:7]=1[S:13]([NH:16][C:17]1[C:22]([O:4][CH2:1][C:2]#[CH:3])=[N:21][C:20]([Cl:24])=[CH:19][N:18]=1)(=[O:15])=[O:14]

Participants

3

Reactant 2

HCID 7859Propargyl alcoholHCID 101263402,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide

Product 1

HCID 59168181HCID 59168181, compound

Procedure

Prepared by the method of Example 31 using propargyl alcohol (0.3 g) and 2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide (Example 74) (0.35 g). Yield 0.2 g.

Sources & evidence

ORD record
ord-e9bb534493f8466fa81a9d465935d1aa
Source dataset
uspto-grants-2010_02
Patent number
US07662825B2

Reaction notes

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