HCID 22388190, compound → HCID 22388085, compound
Reaction equation
[Cl:1][C:2]1[CH:22]=[C:21](/[CH:23]=[CH:24]/[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:20]=[CH:19][C:3]=1[CH2:4][N:5]1[C:9]2=[N:10][C:11]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][CH:13]=[C:8]2[N:7]=[C:6]1[CH3:18]>CO.C(Cl)(Cl)Cl.[Pt](=O)=O>[Cl:1][C:2]1[CH:22]=[C:21]([CH2:23][CH2:24][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)[CH:20]=[CH:19][C:3]=1[CH2:4][N:5]1[C:9]2=[N:10][C:11]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][CH:13]=[C:8]2[N:7]=[C:6]1[CH3:18]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Methyl 3-(2-chloro-4-(E)-(2-phenylethenyl)benzyl)-2-methyl-3H-imidazo[4,5-b]pyridine-5-carboxylate (2.37 g) was dissolved in methanol/chloroform=1/4 (24 ml), and platinum(IV) oxide (169 mg) was added. The mixture was stirred under a hydrogen atmosphere at normal pressure for 4 hours. Platinum(IV) oxide (169 mg) was added, and the mixture was further stirred under a hydrogen atmosphere at normal pressure for 6 hr. The reaction mixture was filtered through Celite and the filtrate was concentrated to dryness under reduced pressure. The obtained residue was subjected to silica gel column chromatography (eluent: ethyl acetate/chloroform=1/3). The fraction containing the objective compound was concentrated under reduced pressure to give the objective compound (1.92 g) as a white powder.
Workup
- additionwas added
- stirringthe mixture was further stirred under a hydrogen atmosphere at normal pressure for 6 hr
- filtrationThe reaction mixture was filtered through Celite
- concentrationthe filtrate was concentrated to dryness under reduced pressure
- additionThe fraction containing the objective compound
- concentrationwas concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-3024af6402f54515ba9983727a113819
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06348474B1
Reaction notes
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