HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1842738Erstellt: 25. Oktober 2026
1,2-Ethanediamine, N1,N1,N2-trimethyl- → N'-(2-Dimethylaminoethyl)-2-methoxy-N'-methyl-N-[5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-yl]-5-nitrobenzene-1,4-diamine
https://huagongshe.com/reaction/1842738
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Edukt | N-(4-fluoro-2-methoxy-5-nitrophenyl)-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amine | HCID 71239199 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | N'-(2-Dimethylaminoethyl)-2-methoxy-N'-methyl-N-[5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-yl]-5-nitrobenzene-1,4-diamine | HCID 71270206 | 42,1% |
Reaktionsschritte
N1,N1,N2-Trimethylethane-1,2-diamine (221 mg, 2.16 mmol) was added to a suspension of N-(4-Fluoro-2-methoxy-5-nitrophenyl)-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amine (Intermediate 79, 400 mg, 0.98 mmol) in DMA (4 mL). The mixture was heated in a microwave at 140° C. for 0.5 h. The mixture was then concentrated in vacuo and the residue was dissolved in EtOAc (100 mL). This solution was washed with water (2×100 mL) and sat. brine (100 mL), dried (MgSO4) and concentrated in vacuo. Purification by FCC, eluting with 1-8% methanolic ammonia in CH2Cl2 gave the title compound (202 mg, 42%) as an orange dry film; m/z: ES+ MH+ 444.55.
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-109603248e5a4867815cf687e0d059ba |
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| Quellennotiz | uspto-grants-2015_02 |
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