Ethyl 1,2-dimethyl-1H-pyrrole-3-carboxylate → 4,5-Dibromo-2-bromomethyl-1-methyl-1H-pyrrole-3-carboxylic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:10]([Br:11])=[C:9]([Br:12])[N:8]([C:13]2C=CC=CC=2)[C:7]=1[CH2:19][Br:20])=[O:5])[CH3:2].C(OC(C1C=CN(C)C=1C)=O)C>>[CH2:1]([O:3][C:4]([C:6]1[C:10]([Br:11])=[C:9]([Br:12])[N:8]([CH3:13])[C:7]=1[CH2:19][Br:20])=[O:5])[CH3:2]Participants
3
Procedure
Prepared in analogy to that of 4,5-dibromo-2-bromomethyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester from 1,2-Dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester; the title product, 1H NMR (200 MHz, CDCl3): δ (ppm)=4.93 (s, 2H), 4.34 (q, 2H, J=7.1 Hz), 3.69 (s, 3H), 1.40 (t, 3H, J=7.1 Hz).
Sources & evidence
- ORD record
- ord-f267570b36c94d6db6c235281f777812
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696223B2
Reaction notes
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