Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 25051758 | HCID 25051758 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 25051759 | HCID 25051759 | — |
Reaction Steps
1-({[(2-fluoroethyl)amino]carbonyl} amino)-2,3-dihydro-1H-inden-4-yl benzoate (reported earlier, 230 mg, 0.67 mmol) was dissolved in MeOH (20 mL) and lithium hydroxide (900.00 mg, 37.58 mmol) was added. The resulting reaction mixture was refluxed for 4 hours and then cooled to room temperature. Concentration followed by the addition of HCl (10%, 10.00 mL) gave a precipitate. The solid was then washed with water, ether and then vacuum-dried to afford the desired title compound. Spectroscopic data: 1H NMR (300 MHz, DMSO-d6) δ ppm 1.53-1.68 (m, 1H) 2.27-2.41 (m, 1H) 2.47-2.61 (m, 1H) 2.70-2.85 (m, 1H) 3.24-3.39 (m, 2H) 4.31 (t, J=5.13 Hz, 1H) 4.47 (t, J=4.98 Hz, 1H) 4.97-5.10 (m, 1H) 6.03 (t, J=5.57 Hz, 1H) 6.25 (d, J=8.21 Hz, 1H) 6.58-6.72 (m, 2H) 6.97 (t, J=7.77 Hz, 1H) 9.24 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598417B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-386f340d9abb484e9ce9fa422d580ce9 |
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| Source note | uspto-grants-2009_10 |
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