4-Formylphenylboronic Acid → HCID 86599565, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[N:6]([CH2:25][C:26]2[CH:31]=[CH:30][C:29]([S:32]([CH3:35])(=[O:34])=[O:33])=[CH:28][CH:27]=2)[C:7](=[O:24])[C:8]2[C:13]([C:14]=1OS(C(F)(F)F)(=O)=O)=[CH:12][C:11]([Cl:23])=[CH:10][CH:9]=2)=[O:4].[CH:36]([C:38]1[CH:43]=[CH:42][C:41](B(O)O)=[CH:40][CH:39]=1)=[O:37]>>[CH3:1][O:2][C:3]([C:5]1[N:6]([CH2:25][C:26]2[CH:27]=[CH:28][C:29]([S:32]([CH3:35])(=[O:33])=[O:34])=[CH:30][CH:31]=2)[C:7](=[O:24])[C:8]2[C:13]([C:14]=1[C:41]1[CH:42]=[CH:43][C:38]([CH:36]=[O:37])=[CH:39][CH:40]=1)=[CH:12][C:11]([Cl:23])=[CH:10][CH:9]=2)=[O:4]Participants
3
Procedure
The present compound was synthesized by a method similar to that in Example 272 and using 6-chloro-2-(4-methanesulfonylbenzyl)-1-oxo-4-trifluoromethanesulfonyloxy-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester and 4-formylphenylboronic acid.
Workup
- customThe present compound was synthesized by a method similar to that in Example 272
Sources & evidence
- ORD record
- ord-6d08eb9eef0047ea9616fdfe5184cbc2
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07402595B2
Reaction notes
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