Diethyl Malonate → HCID 14875731, compound
Reaction equation
[C:1]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].Br.Br[CH2:14][C:15]1[CH:20]=[CH:19][N:18]=[CH:17][CH:16]=1>>[N:18]1[CH:19]=[CH:20][C:15]([CH2:14][CH:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[C:1]([O:9][CH2:10][CH3:11])=[O:8])=[CH:16][CH:17]=1Participants
3
Procedure
In the same manner as in Example 6 (1), a crude product was obtained using diethyl malonate (6.41 g) and 4-(bromomethyl)pyridine hydrobromide (10.1 g). This was purified by silica gel column chromatography to give the title compound (3.86 g) as an oil.
Workup
- customThis was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-a3186d06b1fd492b961991bef5fa673b
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08461209B2
Reaction notes
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