4-Chloro-5-iodo-2-methylbenzoic acid → 4-Chloro-5-formyl-2-methylbenzoic acid
Reaction equation
C1(C2C([CH:11]=[O:12])=CC(C(N3CCC(C4C=CC(C#N)=CC=4)CC3)=O)=C(C)C=2)CCC1.[Cl:30][C:31]1[C:39](I)=[CH:38][C:34]([C:35]([OH:37])=[O:36])=[C:33]([CH3:41])[CH:32]=1.C1(C2C(C=O)=CC(C(O)=O)=C(C)C=2)CCC1>>[Cl:30][C:31]1[C:39]([CH:11]=[O:12])=[CH:38][C:34]([C:35]([OH:37])=[O:36])=[C:33]([CH3:41])[CH:32]=1Participants
4
Procedure
The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 392.2, except 4-chloro-5-iodo-2-methylbenzoic acid (compound 471.1) was used in place of 4-cyclobutyl-5-iodo-2-methylbenzoic acid (compound 392.1).
Sources & evidence
- ORD record
- ord-b2a401a5e5244c3f9aaed7fb4875d884
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08871790B2
Reaction notes
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