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2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide → 2,3-Dichloro-N-[5-chloro-3-(6-methoxy-3-pyridinylmethoxy)-2-pyrazinyl]benzenesulphonamide

HRID 1444011
Notes
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Reaction equation

HRID 1444011 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([CH2:9][OH:10])=[CH:5][CH:4]=1.[Cl:11][C:12]1[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][C:13]=1[S:19]([NH:22][C:23]1[C:28](Cl)=[N:27][C:26]([Cl:30])=[CH:25][N:24]=1)(=[O:21])=[O:20]>>[Cl:11][C:12]1[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][C:13]=1[S:19]([NH:22][C:23]1[C:28]([O:10][CH2:9][C:6]2[CH:7]=[N:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)=[N:27][C:26]([Cl:30])=[CH:25][N:24]=1)(=[O:21])=[O:20]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 101263402,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamideHCID 12259941(6-Methoxypyridin-3-yl)methanol

Product 1

HCID 102887602,3-Dichloro-N-[5-chloro-3-(6-methoxy-3-pyridinylmethoxy)-2-pyrazinyl]benzenesulphonamide

Procedure

Prepared by the method of Example 31 using (6-methoxy-3-pyridinyl)methanol (0.3 g) and 2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide (Example 74) (0.3 g).

Sources & evidence

ORD record
ord-4458500b3eef475d9b1627cb40cc50f2
Source dataset
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07662825B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes