HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dicyclohexylcarbodiimide → 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-Chlorobenzo(b)thiophene-2-carboxylic Acid | HCID 3854516 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide | HCID 22473892 | 75,2% |
Reaktionsschritte
Stir a mixture of 4-chlorobenzo[b]thiophene-2-carboxylic acid (0.94 g, 4.44 mmol), N,O-dimethylhydroxylamine hydrochloride (0.86 g, 8.87 mmol), DCC (1.1 g, 5.32 mmol) and DIEA (1.43 g, 1.9 mL, 11.08 mmol) in DCM (8 mL) at ambient temperature for 2 hours. Filter the reaction mixture and the filtrate is washed with brine, dried over anhydrous Na2SO4 and concentrated under vacuum. Purify the residue by column chromatography on silica gel eluting with PE:EtOAc (5:1 to 3:1) to afford 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide as white solid (0.85 g, 75.2%). 1H NMR (400 MHz, CDCl3) δ 8.10-8.02 (m, 2H), 7.61-7.51 (m, 2H), 3.84-3.79 (s, 3H), 3.37-3.35 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09255111B2 |
| Quelldatensatz | uspto-grants-2016_02 |
| ORD ID | ord-0c5c0135fd2148cb90970f06943d21b3 |
| Quellennotiz | uspto-grants-2016_02 |