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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1773821Erstellt: 26. Oktober 2026

Dicyclohexylcarbodiimide → 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide

https://huagongshe.com/reaction/1773821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Chlorobenzo(b)thiophene-2-carboxylic AcidHCID 3854516—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamideHCID 2247389275,2%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09255111B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-0c5c0135fd2148cb90970f06943d21b3
Quellennotizuspto-grants-2016_02