5-((Dimethylamino)methyl)-2-furanmethanol → HCID 59168146, compound

HRID 1444056Notes

Reaction equation

HRID 1444056 reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][OH:11])=[CH:7][CH:6]=1)[CH3:3].[Cl:12][C:13]1[C:18]([Cl:19])=[CH:17][CH:16]=[CH:15][C:14]=1[S:20]([NH:23][C:24]1[C:29](Cl)=[N:28][CH:27]=[CH:26][N:25]=1)(=[O:22])=[O:21]>>[Cl:12][C:13]1[C:18]([Cl:19])=[CH:17][CH:16]=[CH:15][C:14]=1[S:20]([NH:23][C:24]1[C:29]([O:11][CH2:10][C:8]2[O:9][C:5]([CH2:4][N:2]([CH3:1])[CH3:3])=[CH:6][CH:7]=2)=[N:28][CH:27]=[CH:26][N:25]=1)(=[O:21])=[O:22]

Participants

3

Reactant 2

HCID 849065-((Dimethylamino)methyl)-2-furanmethanolHCID 591681672,3-Dichloro-N-(3-chloro-2-pyrazinyl)benzenesulphonamide

Product 1

HCID 59168146HCID 59168146, compound

Procedure

Prepared by the method of Example 28 using (5-dimethylaminomethyl-2-furanyl)methanol (0.2 g) and 2,3-dichloro-N-(3-chloro-2-pyrazinyl)benzenesulphonamide (Example 28) (0.4 g). Purified by silica gel chromatography eluting with methanol/dichloromethane mixtures. Yield 0.2 g.

Workup

  1. customPurified by silica gel chromatography
  2. washeluting with methanol/dichloromethane mixtures

Sources & evidence

ORD record
ord-21fa631058404d738b3794690fe02f6e
Source dataset
uspto-grants-2010_02
Patent number
US07662825B2

Reaction notes

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