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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1358498Erstellt: 26. Oktober 2026

Water → 1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamide

https://huagongshe.com/reaction/1358498

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzothiazoloneHCID 13625—
EduktSodium hydrideHCID 24758—
EduktHCID 11164927HCID 11164927—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamideHCID 5701534752,7%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a stirred solution of 2-oxobenzothiazole (83 mg, 0.549 mmol) in DMF (3 ml) was added NaH (60% in mineral oil, 22 mg, 0.549 mmol) at room temperature. After 10 minutes, 1-[(2S,3R)-2-benzyloxy-5-methanesulfonyloxy-3-pentyl]imidazole-4-carboxamide in DMF (3 ml) was added and the resulting mixture was stirred for 6 hours at 60 to 70° C. The reaction mixture was poured into water (30 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (sodium sulfate), and concentrated in vacuo. The residue was purified by silica gel (8 g) column chromatography eluting with chloroform/methanol (100:1 to 30:1) to give 1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamide (63 mg, 52.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06596738B1
Quelldatensatzuspto-grants-2003_07
ORD IDord-7d5460f6e3734611b331b2cca7655c92
Quellennotizuspto-grants-2003_07