HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2390468Erstellt: 24. Oktober 2026
Ammonium Chloride → 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole
https://huagongshe.com/de/reaction/2390468
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | N1-Methyl-4-(trifluoromethyl)benzene-1,2-diamine | HCID 715666 | — |
| Edukt | 3-Fluoroisonicotinaldehyde | HCID 2763003 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole | HCID 66611522 | 62% |
Reaktionsschritte
A mixture of 1.90 g of N1-methyl-4-trifluoromethylbenzene-1,2-diamine, 1.49 g of 3-fluoropyridine-4-carbaldehyde, 3.12 g of sodium bisulfite and 20 ml of DMF was stirred for 1.5 hours while heating at 80° C., then, was stirred for 2 hours while heating at 120° C. After cooling down to room temperature, a saturated ammonium chloride aqueous solution was poured, and the mixture was extracted three times with ethyl acetate. The combined organic layers were dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.83 g of 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 4).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08273764B2 |
|---|
| Quelldatensatz | uspto-grants-2012_09 |
|---|
| ORD ID | ord-322696cc977e4e8d843e9d0710be5298 |
|---|
| Quellennotiz | uspto-grants-2012_09 |
|---|