Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 58724142 | HCID 58724142 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58724181 | HCID 58724181 | 65% |
Reaction Steps
(R)-1-(5-(3-(dimethylamino)pyrrolidin-1-ylsulfonyl)indolin-1-yl)ethanone was dissolved in THF. A 2 N HCl solution of equal volume was added, and the reaction mixture was stirred at 60° C. for 1 h. Volatiles were removed in vacuo, and the product that was precipitated was collected on a fritted glass funnel, washed with water, and was dried in vacuo at 45° C. overnight to obtain the title compound in 65% yield. 1H NMR (300 MHz, MeOD) δ ppm 2.02-2.22 (m, 1 H) 2.25-2.47 (m, 1 H) 2.88 (s, 6 H) 3.14-3.26 (m, 1 H) 3.28-3.33 (m, 2 H) 3.34-3.64 (m, 4 H) 3.82-4.01 (m, 2 H) 7.51-7.60 (m, 1 H) 7.87 (d, J=8.67 Hz, 1 H) 7.93 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759339B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-2f890220b8614fe8afb75c30a8f54dbf |
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| Source note | uspto-grants-2010_07 |
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