Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86702031 | HCID 86702031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68176377 | HCID 68176377 | — |
Reaction Steps
To a solution of indole (1 eq.) in THF is added NaH (1.5 eq., 60% in oil) and the mixture is stirred at 20° C. for 1 h. A solution of 4-[(4-Chloro-benzyl)-(1-chlorocarbonyl-2-methyl-azetidine-2-carbonyl)-amino]-butyric acid methyl ester in THF in added dropwise and the mixture is stirred at 20° C. for 16 h. The mixture was concentrated and the residue dissolved in EtOAc, washed with aqueous HCl (0.1N), a saturated aqueous solution of NaHCO3 and brine. The organic layer is dried over Na2SO4, filtered and concentrated under reduced pressure. The crude residue is used as such in next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759334B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-b60265b0d6754cedbd67f0f08a1ff394 |
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| Source note | uspto-grants-2014_06 |
|---|