HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582967Erstellt: 26. Oktober 2026
Dimethylformamide → N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylchloroacetamide
https://huagongshe.com/reaction/1582967
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Chloroacetyl chloride | HCID 6577 | — |
| Edukt | 3-(3-Chlorobenzoyl)-2-ethylamino-6-methylpyridine | HCID 11054902 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylchloroacetamide | HCID 22716666 | — |
Reaktionsschritte
To a DMF solution of 3-(3-chlorobenzoyl)-2-ethylamino-6-methylpyridine were added chloroacetyl chloride and pyridine, followed by reaction at room temperature. Thereafter, the whole was worked up and purified in a usual manner to obtain N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]—N-ethylchloroacetamide. To an acetonitrile solution of the compound were added N-tert-butoxycarbonylpiperazine and potassium carbonate, followed by reaction under heating. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain 2-[4-tert-butoxycarbonylpiperazin-1-yl]—N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylacetamide. The resulting compound was reacted with sodium methoxide in methanol under heating. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain 3-(1 -tert-butoxycarbonylpiperazin-4-yl)-4-(3-chlorophenyl)-1-ethyl-7-methyl-1,8-naphthyridin-2(1H)-one. NMR1: 4.73 (2H, q, J=7.3 Hz), 3.15-3.35 (2H, m), 1.38 (9H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06740662B1 |
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| Quelldatensatz | uspto-grants-2004_05 |
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| ORD ID | ord-2b7066718f6d4a3d956f6504ca1831b0 |
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| Quellennotiz | uspto-grants-2004_05 |
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