HCID 11149822, compound → HCID 18331717, compound
Reaction equation
C(OC(N[C:8]1[CH:12]=[CH:11][S:10][C:9]=1/[C:13](=[CH:15]/[CH:16]([CH3:18])[CH3:17])/[CH3:14])=O)(C)C.[CH:19]([O:22][C:23](NC1C=CSC=1/C(=C\C(C)C)/C)=[O:24])([CH3:21])[CH3:20].C(OC(NC1C=CSC=1C(CC(C)C)=C)=O)(C)C>[C].[Pd].CO>[CH:19]([O:22][C:23]([C:8]1[CH:12]=[CH:11][S:10][C:9]=1[CH:13]([CH3:14])[CH2:15][CH:16]([CH3:17])[CH3:18])=[O:24])([CH3:21])[CH3:20]Participants
Procedure
2.06 g (7.72 mmol) of the mixture of 3-isopropoxycarbonylamino-{2-(E)-(4-methyl-2-penten-2-yl)}thiophene, 3-isopropoxycarbonylamino-{2-(Z)-(4-methyl-2-penten-2-yl)}thiophene, and 3-isopropoxycarbonylamino-{2-(4-methyl-1-penten-2-yl) }thiophene obtained in Example 13 and 0.41 g of 5% palladium carbon (Degussa chemical catalyst E106R/W) were charged into 20 ml of methanol, and after nitrogen purge, a hydrogenation reaction was conducted at normal pressure under hydrogen atmosphere for 9 hours. After nitrogen purge, the catalyst was filtrated off, and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1) to obtain 1.61 g of the intended compound as a colorless crystal (yield: 70%).
Workup
- customafter nitrogen purge
- customa hydrogenation reaction
- customAfter nitrogen purge
- filtrationthe catalyst was filtrated off
- distillationthe solvent was distilled off under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1)
Sources & evidence
- ORD record
- ord-14c1bd2cbd79493699d505f09651e037
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06239282B1
Reaction notes
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