HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270700Erstellt: 25. Oktober 2026
Methyl iodide → 2(1h)-Quinolinone,3-(2,6-dichloro-3-nitrophenyl)-1-methyl-
https://huagongshe.com/reaction/270700
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | 3-(2,6-dichloro-3-nitro-phenyl)-1H-quinolin-2-one | HCID 59833933 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2(1h)-Quinolinone,3-(2,6-dichloro-3-nitrophenyl)-1-methyl- | HCID 59833808 | 35,8% |
Reaktionsschritte
To a solution of 3-(2,6-dichloro-3-nitro-phenyl)-1H-quinolin-2-one (0.21 g, 0.6266 mmol) in DMF (5.0 mL) is added HNa (30.1 mg, 60%, 0.752 mmol) and IMe (120.1 mg, 0.846 mmol) at 0° C. After the mixture is stirred for two hours at 0° C., the mixture is diluted with EtOAc and washed with saturated K2CO3, brine and water. The organic layer is dried, filtered and concentrated to give crude product, which is purified by flash silica gel column, eluting with CH2Cl2 (100%) gradient to CH2Cl2/MeOH (2N NH3) (95/5), t give the titled intermediate as a solid (78 mg, 35.8%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07449582B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-60dd77d7c65f4499bcef4f71040252c5 |
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| Quellennotiz | uspto-grants-2008_11 |
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