Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | HCID 68227316 | HCID 68227316 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68227475 | HCID 68227475 | 61.2% |
Reaction Steps
2.2 g of isoindoline are added to 5.9 g of tert-butyl 5-(2-ethoxy-2-oxoethyl)-2,3-dioxoindoline-1-carboxylate in 100 ml of tetrahydrofuran, and the mixture is subsequently stirred at 23° C. for 1 h. The solvent is removed in vacuo, and the residue is purified by column chromatography, giving 4.9 g of ethyl 2-[4-(tert-butoxycarbonylamino)-3-(2-isoindolin-2-yl-2-oxoacetyl)phenyl]acetate;
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-b89296b670e64a9db1941dfd3d54c616 |
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| Source note | uspto-grants-2014_12 |
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