Methyl 3-formyl-4,5-dimethyl-1H-pyrrole-2-carboxylate → HCID 54460326, compound

HRID 1107805Notes

Reaction equation

HRID 1107805 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].CS(O[CH2:19][CH:20]=[CH:21][C:22]([F:25])([F:24])[F:23])(=O)=O>>[CH:1]([C:3]1[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]([CH2:19][CH:20]=[CH:21][C:22]([F:25])([F:24])[F:23])[C:4]=1[C:10]([O:12][CH3:13])=[O:11])=[O:2]

Participants

3

Reactant 2

HCID 10773740Methyl 3-formyl-4,5-dimethyl-1H-pyrrole-2-carboxylateHCID 53958317HCID 53958317, compound

Product 1

HCID 54460326HCID 54460326, compound

Procedure

The title compound (trans) was prepared as a pale yellow oil in 60.0% yeild in a similar procedure to that described in Referential Example 9 by using methyl 3-formyl-4,5-dimethylpyrrole-2-carboxylate and 4,4,4-trifluoro-2-butenyl methanesulfonate (trans).

Sources & evidence

ORD record
ord-ceafdd1a56b24ccaa770d6fc2cce229d
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Reaction notes

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