Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 59441931 | HCID 59441931 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 59441889 | HCID 59441889 | — |
Reaction Steps
To a solution of 1-{3-[4-(1-methylethyl)-1-piperazinyl]propanoyl}-5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (0.62 g, 1.65 mmol) in absolute ethanol (150 mL) and DMA (10 mL) was added tin (II) chloride dihydrate (2.23 g, 7.84 mmol) and 1M HCl(3.0 mL). After overnight stirring, reaction was quenched with excess saturated NaHCO3 solution, stirred for one hr, and filtered through a celite pad which was rinsed with methanol. After organic solvent removal, the aqueous layer was extracted with dichloromethane (2×200 mL), the organic layers were combined, adsorbed to silica gel and purified by column chromatography (DCM to 5% MeOH/DCM+0.1% NH4OH) to afford 1-{3-[4-(1-methylethyl)-1-piperazinyl]propanoyl}-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine. ESIMS (M+H)+=347.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-12e628b24a6b46a7b4f695ab0ce6b1e6 |
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| Source note | uspto-grants-2011_07 |
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