Methyl 3-cyano-5-methyl-1H-pyrrole-2-carboxylate → 4-Bromo-3-cyano-5-methyl-1H-pyrrole-2-carboxylic acid
Reaction equation
[Br:1][C:2]1[C:3]([C:12]#[N:13])=[C:4]([C:9]([OH:11])=[O:10])[NH:5][C:6]=1[CH2:7]C.COC(C1NC(C)=CC=1C#N)=O>>[Br:1][C:2]1[C:3]([C:12]#[N:13])=[C:4]([C:9]([OH:11])=[O:10])[NH:5][C:6]=1[CH3:7]Participants
3
Procedure
The title compound was prepared by a procedure analogous to Intermediate 33 starting from 3-cyano-5-methyl-1H-pyrrole-2-carboxylic acid methyl ester (Intermediate 28).
Sources & evidence
- ORD record
- ord-5eaf1417fcfe44f18fbfd538b2a12863
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709503B2
Reaction notes
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