HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667428Erstellt: 25. Oktober 2026
Binap, (A+-)- → 4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one
https://huagongshe.com/reaction/1667428
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 3-Piperidin-1-ylmethyl-benzylamine | HCID 2794678 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Edukt | 6-Bromo-4-chlorophthalazin-1(2H)-one | HCID 53308487 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one | HCID 58447352 | — |
Reaktionsschritte
A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (70 mg, 0.27 mmol), 3-piperidin-1-ylmethyl-benzylamine (72 mg, 0.35 mmol), Pd2(dba)3 (25 mg, 0.027 mmol), rac-BINAP (51 mg, 0.081 mmol) and NaOt-Bu (76 mg, 0.81 mmol) in DMA (6 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one: 16 mg (15.5%): m/z (M+H)=383. 1H-NMR (DMSO-d6) δ: 12.30 (s, 1H), 7.95 (d, 1H), 7.63 (m, 1H), 7.25 (m, 3H), 7.15 (m, 2H), 6.75 (s, 1H), 4.41 (d, 2H), 3.37 (s, 2H), 2.24 (m, 4H), 1.38 (m, 4H), 1.32 (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08044041B2 |
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| Quelldatensatz | uspto-grants-2011_10 |
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| ORD ID | ord-abf262d810e54e39bd412ecdac26a62c |
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| Quellennotiz | uspto-grants-2011_10 |
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