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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1614151Erstellt: 24. Oktober 2026

Triethylamine → 3,3a, 4,5-Tetrahydro-3a-methoxycarbonyl-N-[4-(trifluoromethyl)phenyl]-N-[N'-(1-methylethyl)-N'-(ethoxycarbonyl)aminosulfenyl]-2H-benz[g]indazole-2-carboxamide

https://huagongshe.com/de/reaction/1614151

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3,3a,4,5-tetrahydro-3a-methoxycarbonyl-N-[4'-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamideHCID 18988349—
EduktEthyl (chlorosulfenyl)(1-methylethyl)carbamateHCID 20139494—
LösungsmittelDichloromethaneHCID 6344—
Produkt3,3a, 4,5-Tetrahydro-3a-methoxycarbonyl-N-[4-(trifluoromethyl)phenyl]-N-[N'-(1-methylethyl)-N'-(ethoxycarbonyl)aminosulfenyl]-2H-benz[g]indazole-2-carboxamideHCID 8839671585,7%

Reaktionsschritte

To a solution of the title compound of Step B (2.0 g, 4.8 mmol) in 50 ml methylene chloride cooled to 0° C. was added triethylamine (1.0 g, 0.01 mol) and ethyl (chlorosulfenyl)(1-methylethyl)carbamate from Step D (1.4 g, 7.7 mmol). The mixture was allowed to warm to room temperature and stirred for one hour. The crude mixture was purified by silica column chromatography using ether-hexane (1:2) as eluent. The title compound (2.38 g) was obtained in about 90% purity (mp: 130°-134°). Extraction of the product with ether-hexane (2:1) gave 1.8 g of a highly pure material mp: 139°-140° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05196408
Quelldatensatzuspto-grants-1993_03
ORD IDord-cd5e9a4d26844e49bf100448687b566e
Quellennotizuspto-grants-1993_03