Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 117628758 | HCID 117628758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89535667 | HCID 89535667 | — |
Reaction Steps
To a solution of tert-butyl 6-[(3-methoxy-3-oxopropyl)sulfonyl]-1H-indole-1-carboxylate (400 mg, 1.13 mmol) in THF (5.5 mL) was added sodium methoxide (2.26 mL, 0.5 M, 1.13 mmol). The reaction mixture was stirred for 20 minutes, then the solvents were removed under reduced pressure and the residue was stripped down from heptanes to generate a white foam. This foam was suspended in DCM (5.5 mL) at 0° C. and then NCS (151 mg, 1.13 mmol) was added and the reaction mixture was stirred for 1 hour. The reaction was quenched by the addition of brine (4 mL) and the phases were separated using a phase separator. The aqueous layer washed with DCM. The combined organics were concentrated under reduced pressure. The crude was purified on silica gel eluting with hexanes and ethyl acetate to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133157B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-24c6844373534f0ebbd775e29e3de069 |
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| Source note | uspto-grants-2015_09 |
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