Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 25057387 | HCID 25057387 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68458293 | HCID 68458293 | — |
Reaction Steps
A solution of (R)-4-(benzyloxy)-1-(1-(2-(3-fluoropyrrolidin-1-yl)ethyl)-1H-indazol-5-yl)pyridin-2(1H)-one (10.5 mg, 0.024 mmol) in CH2Cl2 (0.3 mL) was treated with anhydrous HCl in diethyl ether (24 μL, 0.024 mmol, 1.0 M). After stirring at ambient temperature for 2.0 h, the reaction mixture was concentrated, dissolved in CH3CN and H2O, partially concentrated, and then lyophilized to yield the title compound (11.9 mg, quantitative) as an off white solid: 1H NMR (500 MHz, DMSO-d6) δ 10.58 (br s, 0.5H), 8.24 (s, 1H), 7.84 (d, J=9.0 Hz, 1H), 7.79 (s, 1H), 7.60 (d, J=7.5 Hz, 1H), 7.48-7.36 (m, 6H), 6.12 (dd, J=8.0, 3.0 Hz, 1H), 5.99 (d, J=2.5 Hz, 1H), 5.53-5.39 (m, 1H), 5.15 (s, 2H), 4.87 (s, 2H), 3.88-3.51 (m, 5H), 3.21-3.16 (m, 1H), 2.15-2.08 (m, 1H), 1.30-1.23 (m, 1H); ESI MS m/z 433 [M+H]+, HPLC (Method A)>99.0% (AUC), tR=14.1 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268868B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-bb48fbef8f6d4876b10d32570747594c |
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| Source note | uspto-grants-2012_09 |
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