Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 70873808 | HCID 70873808 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70873687 | HCID 70873687 | 91% |
Reaction Steps
To a solution of methyl 5-chloro-3-[ethyl(oxan-4-yl)amino]-2-methoxybenzoate (127 mg, 0.39 mmol) in THF (4 ml) was added 4M NaOH (3.87 ml). The reaction mixture was stirred at 50° C. for 24 hours. The reaction mixture was acidified to pH 2-3 with 6M HCl and extracted with DCM (5×15 ml). The combined organic extracts were dried over MgSO4, filtered and concentrated under reduced pressure to give 111 mg (91%) of the title compound as a yellow oil. LC-MS 80%, 1.25 min (3 minute LC-MS method), m/z=314.4/315.9, 1H NMR (500 MHz, Chloroform-d) δ ppm 10.02-9.55 (m, 1H), 8.01-7.47 (m, 1H), 7.36-6.96 (m, 1H), 4.15-3.86 (m, 5H), 3.76 (t, J=6.6 Hz, 2H), 3.55-3.12 (m, 3H), 1.95-1.59 (m, 4H), 1.15-0.88 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376422B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-5ad6e91e9d924e3f90817b34078cd933 |
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| Source note | uspto-grants-2016_06 |
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