Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | HCID 67154038 | HCID 67154038 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67154064 | HCID 67154064 | 24% |
Reaction Steps
584 mg of isoindoline are added to 2.4 g of 5-[1-(3,3-difluoropropyl)-1-ethoxycarbonyl-4,4-difluorobutyl]-1-tert-butoxycarbonyl-2,3-dioxoindoline in 30 ml of tetrahydrofuran, and the mixture is subsequently stirred at 23° C. for 1 h. The mixture is evaporated to dryness in vacuo and purified by column chromatography, giving 700 mg (24%) of ethyl 2-[4-(tert-butoxycarbonylamino)-3-(2-isoindolin-2-yl-2-oxoacetyl)phenyl]-2-(3,3-difluoropropyl)-5,5-difluoropentanoate;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906930B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-2c9398d2eb0a4588adbd7764753f1b90 |
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| Source note | uspto-grants-2014_12 |
|---|