HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091767Generated: November 2, 2026
Diisopropylethylamine → 4-(3-(4-(2-(dimethylamino)ethoxy)piperidine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one
https://huagongshe.com/reaction/1091767
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Fluoro-5-[(4-oxo-3,4-dihydrophthalazin-1-yl)methyl]benzoic acid | HCID 24811740 | — |
| Reactant | Dimethyl(2-(piperidin-4-yloxy)ethyl)amine | HCID 43167826 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-(4-(2-(dimethylamino)ethoxy)piperidine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one | HCID 57791855 | 28.7% |
Reaction Steps
2-fluoro-5-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoic acid (1) (0.2 g, 0.67 mmol), N,N-dimethyl-2-(piperidin-4-yloxy)ethanamine (85) (0.116 g, 0.67 mmol) and 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate (0.215 g, 0.67 mmol) were dissolved in DMF (10 mL), to this was added DIPEA (0.117 mL, 0.67 mmol) and the reaction was stirred for 1 hour. The solvent was evaporated to dryness and the gum was dissolved in acetonitrile (4 mL). The crude product was purified by preparative HPLC (Waters XBridge Prep C18 OBD column, 5μ silica, 19 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the desired material as a white solid (0.087 g, 28.7% yield); 1H NMR (400.132 MHz, CDCl3) δ 1.62-1.51 (1H, m), 1.84-1.66 (3H, m), 1.95-1.89 (1H, m), 2.28 (6H, s), 2.52 (2H, t), 3.15-3.01 (1H, m), 3.48-3.40 (1H, m), 3.62-3.51 (3H, m), 4.07-3.98 (1H, m), 4.27 (2H, s), 7.01 (1H, t), 7.32-7.25 (2H, m), 7.77-7.70 (3H, m), 8.47-8.45 (1H, m), 10.62 (1H, s); m/z (LC-MS, ESI+), RT=1.67 (M+H 452).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129380B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-c37055a9189746289f0b12aa5ab87261 |
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| Source note | uspto-grants-2012_03 |
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