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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25571Erstellt: 24. Oktober 2026

Sodium Iodide → HCID 178483981, Verbindung

https://huagongshe.com/de/reaction/25571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktSodium hydrideHCID 24758—
EduktCaptamine HydrochlorideHCID 25798—
EduktPotassium bisulfateHCID 516920—
EduktEther sodium bicarbonateHCID 23682952—
EduktHCID 178484820HCID 178484820—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178483981HCID 17848398163%

Reaktionsschritte

A solution of 280 mg (0.5 mmol) of trans-4-Trifluoromethyl-benzenesulfonic acid 4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexylmethyl ester and 78 mg (0.55 mmol) of 2-dimethylaminoethanethiol hydrochloride in 4.5 ml DMF was treated at 0° C. with 48 mg (1.1 mmol) of 55% NaH, stirred for 20 h at RT. After cooling (0° C.) and treatment with a catalytic amount of NaI followed by 78 mg (0.55 mmol) of 2-dimethylaminoethanethiol hydrochloride and 48 mg (1.1 mmol) of 55% NaH the reaction mixture was stirred for 18 h at RT. The reaction was neutralized (aqueous 10% KHSO4, at 0° C.) and poured into aqueous sat. NaHCO3/Et2O (3×). The organic phases were washed with aqueous 10% NaCl solution, dried over Na2SO4 and evaporated. Purification by flash column chromatography on silica gel with CH2Cl2/MeOH (95:5) yielded 138 mg (63%) of trans-N-[4-(2-Dimethylamino-ethylsulfanylmethyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide, MS: 439 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858651B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-b359497fad8842908e41ec30d66d9a0f
Quellennotizuspto-grants-2005_02