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HRID 79124Erstellt: 24. Oktober 2026
1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → 9-cyclopentyl-N-(6-(4-(dimethylamino)-1-piperidinyl)-3-pyridinyl)-9H-pyrido[4',3':4,5]-pyrrolo[2,3-d]pyrimidin-2-amine
https://huagongshe.com/de/reaction/79124
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Edukt | 1-(5-bromopyridin-2-yl)-N,N-dimethylpiperidin-4-amine | HCID 58299576 | — |
| Edukt | 9-Cyclopentyl-9H-pyrido[4',3':4,5]pyrrolo[2,3-d]pyrimidin-2-amine | HCID 58299585 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 9-cyclopentyl-N-(6-(4-(dimethylamino)-1-piperidinyl)-3-pyridinyl)-9H-pyrido[4',3':4,5]-pyrrolo[2,3-d]pyrimidin-2-amine | HCID 58299645 | 27,7% |
Reaktionsschritte
To a microwave reaction vessel were placed compound 4 (30 mg, 118 μmmol), compound 91 (50 mg, 178 μmol), tris(dibenzylideneacetone)dipalladium (0) (5.4 mg, 5.9 μmol), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (8.6 mg, 15 μmol), and sodium tert-butoxide (34 mg, 355 μmol). 1,4-dioxane (4 mL) was added and the vessel was purged with N2 for 3 min, then capped and subjected to microwave irradiation for 2 h at 120° C. After removal of the volatiles, the residue was dissolved in methanol and filtered. The filtrate was subjected to reverse phase preparative HPLC (acetonitrile/water containing 0.1% TFA each, 40 min from 5 to 40%) to give ˜15 mg of compound 90 as a TFA salt. 1H NMR (400 MHz, CD3OD) δ 9.43 (1 H, s), 9.16 (1 H, s), 8.65 (1 H, d, J=2.3 Hz), 8.48-8.57 (2 H, m), 8.12 (1 H, dd, J=9.4, 2.3 Hz), 7.21 (1 H, d, J=9.4 Hz), 5.29-5.47 (1 H, m), 4.45 (2 H, d, J=13.7 Hz), 3.49-3.58 (1 H, m), 3.03-3.18 (2 H, m), 2.92 (6 H, s), 2.37-2.54 (2 H, m), 2.04-2.29 (6 H, m), 1.76-1.93 (4 H, m) ppm; LCMS-ESI (POS), M/Z, M+1: Found 457.3, Calculated 457.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841312B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-698c0771991f49f1b35e0d90ac18160b |
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| Quellennotiz | uspto-grants-2014_09 |
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