Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86724075 | HCID 86724075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86724076 | HCID 86724076 | 56.3% |
Reaction Steps
A mixture of methyl 2-[4-(2,4-dichlorophenyl)-1-methyl-3-(2-pyridyl)-6,7-dihydro-4H-pyrazolo[3,4-e][1,4]thiazepin-8-yl]acetate (0.300 g, 0.64 mmol) and lithium hydroxide (0.062 g, 2.6 mmol) in THF (10 mL) and water (5 mL) was stirred at rt for about 2 h. Then 1 M aqueous HCl (15 mL) was added and the mixture was extracted with ethyl acetate (2×25 mL). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by prep-HPLC (Table 2, Method a) to give 2-[4-(2,4-dichlorophenyl)-1-methyl-3-(2-pyridyl)-6,7-dihydro-4H-pyrazolo[3,4-e][1,4]thiazepin-8-yl]acetic acid (0.160 g, 0.36 mmol, 56%) as a white solid: LC-MS (Table 1, Method b) Rt=6.57 min; m/z 449 (M+H)+; 1H-NMR (CDCl3, Bruker 400 MHz) δ 2.73-2.91 (2 H, m) 3.40-3.63 (2 H, m) 3.92 (3 H, s) 4.12 (1 H, d, J=18.4 Hz) 4.21 (1 H, d, J=18.4 Hz) 5.95 (1 H, br s) 6.46 (1 H, s) 6.94 (1 H, d, J=8.4 Hz) 7.00-7.07 (2H, m) 7.40 (1H, d, J=2.1Hz) 7.58 (1H, td, J=7.5, 1.8 Hz) 7.72 (1H, d, J=7.9 Hz) 8.40 (1H, d, J=5.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150592B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-5cbd14a485fe4126aa25213396261286 |
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| Source note | uspto-grants-2015_10 |
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