Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86618245 | HCID 86618245 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86618244 | HCID 86618244 | 80% |
Reaction Steps
2-Methyl-1-(phenylsulfonyl)-1H-indole-4-carbaldehyde (94 mg, 0.3 mmol, Intermediate 47) was dissolved in THF (dry) (4 mL) before boc-piperazine (87.7 mg, 0.5 mmol) was added followed by acetic acid (188 mg, 3.1 mmol) and sodium triacetoxyborohydride (199 mg, 0.9 mmol) was added. The reaction mixture was heated in microwave for 720 s at 130° C. The solvent was evaporated, added water and DCM. Separated the phases and extracted the aqueous phase with DCM twice. The combined organic phases were dried (MgSO4) and the solvent was evaporated. The crude product was purified by preparative HPLC (30-60). Isolated 110 mg, as an oil, yield 80%. MS (ESI+) for C25H31N3O4S m/z 470 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812017B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-52163f3834b24069ae78b5187c108268 |
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| Source note | uspto-grants-2010_10 |
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