3-Chloro-2-methyl-1-propene → HCID 18785598, compound
Reaction equation
[CH:1]([C:3]1[C:7]([CH3:8])=[C:6]([CH3:9])[NH:5][C:4]=1[C:10]([O:12][CH3:13])=[O:11])=[O:2].Cl[CH2:15][C:16]([CH3:18])=[CH2:17]>>[CH:1]([C:3]1[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]([CH2:17][C:16]([CH3:18])=[CH2:15])[C:4]=1[C:10]([O:12][CH3:13])=[O:11])=[O:2]Participants
3
Procedure
The title compound was prepared as a pale yellow oil in 86.2% yeild in a similar procedure to that described in Referential Example 9 by using but using methyl 3-formyl-4,5-dimethylpyrrole-2-carboxylate and 3-chloro-2-methyl-1-propene.
Sources & evidence
- ORD record
- ord-e3d5d60c8e594b53bf97b1d59b9763c5
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06063782
Reaction notes
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