Fluoromethyl 4-methylbenzenesulfonate → HCID 59370024, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([N:8]2[CH:13]=[CH:12][C:11](=[O:14])[C:10]([C:15]3[N:16]([C:20]4[C:29]5[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=5)[CH:23]=[CH:22][CH:21]=4)[N:17]=[CH:18][CH:19]=3)=[N:9]2)[CH:5]=[CH:6][CH:7]=1.S(C1C=CC(C)=CC=1)(O[CH2:34][F:35])(=O)=O>>[F:35][CH2:34][O:1][C:2]1[CH:3]=[C:4]([N:8]2[CH:13]=[CH:12][C:11](=[O:14])[C:10]([C:15]3[N:16]([C:20]4[C:29]5[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=5)[CH:23]=[CH:22][CH:21]=4)[N:17]=[CH:18][CH:19]=3)=[N:9]2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The product was obtained starting from 1-(3-Hydroxy-phenyl)-3-(2-naphthalen-1-yl-2H-pyrazol-3-yl)-1H-pyridazin-4-one (example 276) and fluoromethyl tosylate according to the method described in example 290. MS: M=413.1 (M+H)+
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-a5281d41213e4ab4adf32348d660b75d
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178538B2
Reaction notes
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