3-Chloro-4-methanesulfonylaniline → 3-Hydroxymethyl-4-(methylsulfonyl)phenylhydrazine hydrochloride
Reaction equation
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][C:9]=1[S:10]([CH3:13])(=[O:12])=[O:11])[NH2:6].[Cl:14]C1C=C(C=CC=1S(C)(=O)=O)[NH2:18]>>[ClH:14].[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([NH:6][NH2:18])[CH:7]=[CH:8][C:9]=1[S:10]([CH3:13])(=[O:12])=[O:11]Participants
3
Procedure
The title compound was prepared according to the procedure of step1 of Example 155 using 3-hydroxymethyl-4-(methylsulfonyl)aniline from step3 instead of 3-chloro-4-(methylsulfonyl)aniline.
Sources & evidence
- ORD record
- ord-824616f7c1c14d3d8a5060f38bc503e5
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727238B2
Reaction notes
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