HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1842720Erstellt: 27. Oktober 2026
Diisopropylethylamine → 5-Chloro-N-{4-[(3S)-3-dimethylaminopyrrolidin-1-yl]-2-methoxy-5-nitrophenyl}-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine
https://huagongshe.com/reaction/1842720
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | (3S)-(-)-3-(Dimethylamino)pyrrolidine | HCID 7019156 | — |
| Edukt | 5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine | HCID 71239348 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 5-Chloro-N-{4-[(3S)-3-dimethylaminopyrrolidin-1-yl]-2-methoxy-5-nitrophenyl}-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine | HCID 71270260 | 98,2% |
Reaktionsschritte
(3S)—N,N-Dimethylpyrrolidin-3-amine (0.092 mL, 0.72 mmol) was added to a suspension of 5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine (Intermediate 20, 250 mg, 0.60 mmol) and DIPEA (0.125 mL, 0.72 mmol) in DMA (3 mL) and the mixture was heated at 140° C. in a microwave for 0.5 h. The mixture was then diluted with CH3OH and absorbed onto an SCX column. The column was washed with CH3OH and then eluted with 1:1 7M methanolic ammonia in CH2Cl2. Appropriate fractions were concentrated and further purification by FCC, eluting with 2% 7N methanolic ammonia in CH2Cl2 gave the title compound (300 mg, 98%) as an orange foam; 1H NMR: 1.75-1.95 (1H, m), 2.09-2.30 (7H, m), 2.72-2.87 (1H, m), 3.11-3.27 (3H, m), 3.42-3.56 (1H, m), 3.90 (3H, s), 6.57 (1H, s), 7.13 (1H, t), 7.26-7.41 (1H, m), 8.09 (1H, s), 8.28-8.50 (2H, m), 8.67 (1H, s), 8.84 (1H, d), 8.95 (1H, s); m/z: ES+ MH+ 509.5.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08946235B2 |
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| Quelldatensatz | uspto-grants-2015_02 |
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| ORD ID | ord-ef1ecd15b08d4f58bdb9b548f0b81814 |
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| Quellennotiz | uspto-grants-2015_02 |
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