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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13123Erstellt: 24. Oktober 2026

Diisopropylamine → S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate

https://huagongshe.com/de/reaction/13123

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukt3,4,7,8-Tetramethyl-1,10-phenanthrolineHCID 74265—
Edukt1-(4-fluorophenyl)-5-iodo-1H-indazoleHCID 59251128—
EduktHCID 178526132HCID 178526132—
KatalysatorHCID 178505377HCID 178505377—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
ProduktS-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioateHCID 5933984820%

Reaktionsschritte

To a solution of 1-(4-fluorophenyl)-5-iodo-1H-indazole (103e, 0.224 g, 0.66 mmol), thiobenzoic acid (0.093 ml, 0.79 mmol), 3,4,7,8-tetramethyl-1,10-phenantroline (0.031 g, 0.13 mmol) and N,N-diisopropylamine (0.220 ml, 1.32 mmol) in toluene (2.5 ml) was added copper(I) iodine (2.245 μl, 0.07 mmol). The resulting mixture was stirred at 110 C O/N. The reaction mixture was cooled to r.t. diluted with EtOAc and washed with water. The organic phase was the dried the solvent evaporated and then purified on HPLC. The relevant fractions were collected freezdried to give 45 mg of product (20% yield) which was analysed by LC/MS.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728030B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5b1dc549e4134f18b2f42ea77cf3f868
Quellennotizuspto-grants-2010_06