Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 2,6-Bis(4-fluorophenyl)pyridine-4-carboxylic acid | HCID 46313701 | — |
| Reactant | HCID 178479612 | HCID 178479612 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178515381 | HCID 178515381 | — |
Reaction Steps
Triethylamine (71.0 μl, 0.51 mol), 1-hydroxybenzotriazole hydrate (35 mg, 0.26 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (49.0 mg, 0.26 mol) were added to an N,N-dimethylformamide solution (0.5 mL) of 2,6-bis(4-fluorophenyl)pyridine-4-carboxylic acid (53.0 mg, 0.17 mmol) and 6-(tetrazol-5-yl)spiro[chroman-2,4′-piperidin]-4-one hydrochloride (82.0 mg, 0.26 mol), and stirred at 60° C. for 3 hours. The reaction liquid was concentrated under reduced pressure, and the resulting residue was purified through high-performance preparative liquid chromatography (0.1% TFA, water/acetonitrile) to obtain the title compound as a white solid. 1H-NMR (400 MHz, DMSO-d6) δ: 8.42 (1H, d, J=2.0 Hz), 8.31 (4H, dd, J=8.7, 5.7 Hz), 8.25 (1H, dd, J=8.7, 2.3 Hz), 7.94 (2H, s), 7.39-7.33 (5H, m), 4.35-4.32 (1H, m), 3.46-3.32 (3H, m), 2.99 (2H, s), 2.13-2.10 (1H, m), 1.91-1.87 (3H, m). MS [M+H]+=579.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138197B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-91ffbacd49964572979697676b988a5e |
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| Source note | uspto-grants-2012_03 |
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