Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178451833 | HCID 178451833 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178518304 | HCID 178518304 | 78% |
Reaction Steps
2-{4-[(1,3-Dioxo-6-thiophen-3-yl-2,3-dihydro-1H-isoquinolin-4-ylidenemethyl)-amino]-phenyl}-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (230 mg, ˜60-70% pure, ˜0.26-0.31 mmol) is mixed with H3PO4 (1 mL) in CH2Cl2 (1 mL) at room temperature. The resulting mixture is stirred until no starting material is detected by TLC. CH3CN and H2O and ice were then added to dilute the sample. The mixture is neutralized by NaOH and extracted with EtOAc. The EtOAc layer is washed with brine and dried. After removal of EtOAc, the residue is purified by flash chromatography to provide the title compound (80 mg, 78% for two steps). 1H NMR (400 MHz, DMSO) δ 12.53 (1H, d, J=12.8 Hz), 11.30 (1H, s), 9.02 (1H, d, J=12.4 Hz), 8.34 (1H, s), 8.21 (1H, s), 8.05 (1H, d, J=7.6 Hz), 7.44-7.85 (7H, m), 5.76-5.84 (2H, m), 3.77-3.81 (1H, m), 3.31-3.50 (2H, m), 2.09-2.21 (2H, m). MS (ESI): 428.1 (M+1)−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713994B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-44fa5330d030486e87793cef03aa7263 |
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| Source note | uspto-grants-2010_05 |
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