5-[4-[2-[4-Methyl-2-propyl-6-oxo-1,6-dihydropyrimidin-1-yl]ethoxy]phenylmethylene]thiazolidine-2,4-dione → 5-[4-[2-[4-methyl-2-Propyl-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]phenyl methyl]thiazolidine-2,4-dione
Reaction equation
[CH3:1][C:2]1[N:3]=[C:4]([CH2:26][CH2:27][CH3:28])[N:5]([CH2:9][CH2:10][O:11][C:12]2[CH:17]=[CH:16][C:15]([CH:18]=[C:19]3[S:23][C:22](=[O:24])[NH:21][C:20]3=[O:25])=[CH:14][CH:13]=2)[C:6](=[O:8])[CH:7]=1.[H][H]>O1CCOCC1.[Pd]>[CH3:1][C:2]1[N:3]=[C:4]([CH2:26][CH2:27][CH3:28])[N:5]([CH2:9][CH2:10][O:11][C:12]2[CH:13]=[CH:14][C:15]([CH2:18][CH:19]3[S:23][C:22](=[O:24])[NH:21][C:20]3=[O:25])=[CH:16][CH:17]=2)[C:6](=[O:8])[CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 5-[4-[2-[4-methyl-2-propyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]phenylmethylene]thiazolidine-2,4-dione (5.0 g, 12.46 mmol) obtained from example 1 in 1,4-dioxane (75 ml) was reduced with hydrogen in the presence of 10% palladium on charcoal (12.0 g) at 60 psi pressure for 40 h. The inure was filtered through a bed of celite. The filtrate was evaporated to dryness under reduced pressure, purified by column chromatography (2:1 EtOAc/petroleum ether as eluent) followed by crystallisation (CH2Cl2) to afford the title compound (4.6 g, 92%), mp 144-146° C.
Workup
- filtrationThe inure was filtered through a bed of celite
- customThe filtrate was evaporated to dryness under reduced pressure
- custompurified by column chromatography (2:1 EtOAc/petroleum ether as eluent)
- customfollowed by crystallisation (CH2Cl2)
Sources & evidence
- ORD record
- ord-0cb0910be93d4b3e97d486f3bdefffc7
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372750B2
Reaction notes
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