5-Amino-2-methoxyphenol → HCID 15550636, compound

HRID 321924Notes

Reaction equation

HRID 321924 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[O:9][CH3:10])[NH2:5].[Br:11][C:12]1[C:17]([F:18])=[C:16]([F:19])[C:15]([F:20])=[C:14]([F:21])[C:13]=1[S:22](Cl)(=[O:24])=[O:23]>>[Br:11][C:12]1[C:17]([F:18])=[C:16]([F:19])[C:15]([F:20])=[C:14]([F:21])[C:13]=1[S:22]([NH:5][C:4]1[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:2]([OH:1])[CH:3]=1)(=[O:24])=[O:23]

Participants

3

Reactant 2

HCID 743145-Amino-2-methoxyphenolHCID 15550635HCID 15550635, compound

Product 1

HCID 15550636HCID 15550636, compound

Procedure

The title compound was prepared in a manner similar to that described in Example 6 of WO 97/30677, beginning with 3-hydroxy-4-methoxyaniline and 2-bromo-3,4,5,6-tetrafluorophenylsulfonyl chloride (Example D, above).

Sources & evidence

ORD record
ord-1932c79a9a214e2db70401b24358e383
Source dataset
uspto-grants-2001_04
Patent number
US06211167B1

Reaction notes

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