Diethyl 2,4-dimethylpyrrole-3,5-dicarboxylate → 1-amino-3,5-dimethyl-1H-pyrrole-2,4-dicarboxylic acid diethyl ester
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]([CH3:17])=[C:9]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:10]=1[CH3:11])=[O:5])[CH3:2].C(OC(C1[N:24](N)C(C(OCC)=O)=CC=1)=O)C>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([NH2:24])[C:8]([CH3:17])=[C:9]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:10]=1[CH3:11])=[O:5])[CH3:2]Participants
3
Procedure
Compound 409A was prepared from 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylic acid diethyl ester by a route analogous to that used for the preparation of compound 406C.
Sources & evidence
- ORD record
- ord-42dab2b9a15648f19d1a263715914735
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07030112B2
Reaction notes
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