Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | HCID 67154049 | HCID 67154049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67154051 | HCID 67154051 | 46% |
Reaction Steps
1.95 g of isoindoline are added to 6.4 g of 5-(1-ethoxycarbonylpentyl)-1-tertbutoxycarbonyl-2,3-dioxoindoline in 100 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 3.8 g (46%) of ethyl 2-[4-(tert-butoxycarbonylamino)-3-(2-isoindolin-2-yl-2-oxoacetyl)phenyl]hexanoate; LC-MS retention time: 2.89 min (“nonpolar” gradient).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08906930B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-eb4034fea70640a9acdfe333361478d3 |
|---|
| Source note | uspto-grants-2014_12 |
|---|
