Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 59490482 | HCID 59490482 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59490563 | HCID 59490563 | — |
Reaction Steps
To a solution of ethyl 3-(4-methoxybenzyl)-6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline-7-carboxylate (159 mg, 0.44 mmol) in tetrahydrofuran (5 mL), methanol (2 mL) and water (3 mL) was added excess lithium hydroxide (0.5 g). The mixture was stirred at room temperature for 1.5 hours diluted with water (50 mL) and extracted with ethyl acetate (3×50 mL). The organic layer was dried with anhydrous magnesium sulfate and evaporated to dryness to give 3-(4-methoxybenzyl)-6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c]isoquinoline-7-carboxylic acid as an off white solid (157 mg). 1H NMR (DMSO-d6) 400 MHz δ 12.33 (brs, 1H), 8.02 (s, 1H), 7.95 (s, 1H), 7.16 (d, J=8.0 Hz, 2H), 6.84 (d, J=8.0 Hz, 2H), 5.52 (s, 2H), 3.69 (s, 3H), 3.14-2.97 (m, 4H), 2.82-2.74 (m, 1H), 2.22-2.14 (m, 1H), 1.97-1.87 (m, 1H); LCMS [M+H]: 338.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263610B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-bfee918717d4424484a1f1b1dc97656a |
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| Source note | uspto-grants-2012_09 |
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