Trimethyl phosphite → Benzyl 2-[4-((E)-2-methoxycarbonylvinyl)-2,6-dimethylphenyl]-1H-indole-6-carboxylate
Reaction equation
[CH3:1][O:2][C:3](/[CH:5]=[CH:6]/[C:7]1[CH:12]=[C:11]([CH3:13])[C:10](/[CH:14]=[CH:15]/[C:16]2[CH:31]=[CH:30][C:19]([C:20]([O:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)=[O:21])=[CH:18][C:17]=2[N+:32]([O-])=O)=[C:9]([CH3:35])[CH:8]=1)=[O:4].P(OC)(OC)OC>>[CH3:1][O:2][C:3](/[CH:5]=[CH:6]/[C:7]1[CH:12]=[C:11]([CH3:13])[C:10]([C:14]2[NH:32][C:17]3[C:16]([CH:15]=2)=[CH:31][CH:30]=[C:19]([C:20]([O:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[O:21])[CH:18]=3)=[C:9]([CH3:35])[CH:8]=1)=[O:4]Participants
3
Conditions
- Temperature
- 110 °C
Procedure
A mixture of benzyl 4-{(E)-2-[4-((E)-2-methoxycarbonylvinyl)-2,6-dimethylphenyl]-vinyl}-3-nitrobenzoate (1.87 g, 3.97 mmol) and trimethyl phosphite (5.0 mL, 5.26 g, 42 mmol) was heated at 110° C. for 3 h. The solvent was removed under reduced pressure and the residue chromatographed using a 10-50% gradient of heptane/ethyl acetate to give the title compound.
Workup
- customThe solvent was removed under reduced pressure
- customthe residue chromatographed
Sources & evidence
- ORD record
- ord-10c4a391f03d4b3686c801ffe36cb7fb
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07879850B2
Reaction notes
Loading…