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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2423189Erstellt: 27. Oktober 2026

o-Toluenesulfonyl chloride → tert-butyl 6-methoxy-1-methyl-8-[(2-methylphenyl)sulfonyl]-1,3,4,8-tetrahydro-2H-[1,4]oxazepino[6,7-e]indole-2-carboxylate

https://huagongshe.com/reaction/2423189

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukto-Toluenesulfonyl chlorideHCID 8623—
EduktSodium hydrideHCID 24758—
Edukttert-Butyl 6-methoxy-1-methyl-1,3,4,8-tetrahydro-2H-[1,4]oxazepino[6,7-e]indole-2-carboxylateHCID 69096461—
KatalysatorWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-butyl 6-methoxy-1-methyl-8-[(2-methylphenyl)sulfonyl]-1,3,4,8-tetrahydro-2H-[1,4]oxazepino[6,7-e]indole-2-carboxylateHCID 6724237911,5%

Reaktionsschritte

tert-Butyl 6-methoxy-1-methyl-1,3,4,8-tetrahydro-2H-[1,4]oxazepino[6,7-e]indole-2-carboxylate (Intermediate 36, 25 mg, 0.059 mmol) was dissolved in DMF (1 mL) and sodium hydride (60% in mineral oil, 4.0 mg, 0.15 mmol) was added. The reaction mixture was stirred at room temperature for 15 minutes before 2-methylbenzenesulfonyl chloride (22 mg, 0.113 mmol) was added. The reaction mixture was allowed to stir at room temperature overnight and a few drops of water were added. The crude product was purified by preparative HPLC (XTerra C18, 50 mM NH4HCO3 pH 10-CH3CN) to give tert-butyl 6-methoxy-1-methyl-8-[(2-methylphenyl)sulfonyl]-1,3,4,8-tetrahydro-2H-[1,4]oxazepino[6,7-e]indole-2-carboxylate (3.3 mg) which was dissolved in DCM (1 mL) and TFA (1 mL) was added. The reaction mixture was stirred at room temperature for 3 hours and evaporated to give the title compound (3.4 mg). MS m/z 387 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07960374B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-8012f81474d04b778235ffad6eef7868
Quellennotizuspto-grants-2011_06