Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67344360 | HCID 67344360 | — |
| Reactant | HCID 178482962 | HCID 178482962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67343811 | HCID 67343811 | 58% |
Reaction Steps
To a solution of methyl 14-cyclohexyl-7-(3-piperazin-1-ylpropyl)-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate (0.11 M) in dry THF was added (tert-butoxycarbonyl){[4-(dimethyliminio)pyridin-1(4H)-yl]sulfonyl}azanide (1 eq) (prepared following literature procedure: Winum, J.-Y. et al Org. Lett. 2001, 3, 2241-2243) and the mixture stirred at 40° C. for 2 h. The reaction was allowed to cool to RT before diluting with EtOAc. The combined organics were washed with 1N HCl (aq), sat. aq. NaHCO3 then brine, dried (Na2SO4), filtered and concentrated in vacuo to afford the product as a yellow foam (58%) that was used without further purification. (ES+) m/z 695 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989438B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-cfc53263109043a3aca365efd94759a3 |
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| Source note | uspto-grants-2011_08 |
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