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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401744Erstellt: 25. Oktober 2026

Water → HCID 57731972, Verbindung

https://huagongshe.com/reaction/401744

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt4-Iodo-N-(thiazol-2-yl)benzenesulfonamideHCID 1019318—
EduktHCID 68534217HCID 68534217—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorHCID 178521658HCID 178521658—
LösungsmittelHydrochloric AcidHCID 313—
ProduktHCID 57731972HCID 57731972—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 4-iodo-N-1,3-thiazol-2-ylbenzenesulfonamide (Preparation 98, 150 mg, 0.41 mmol), (2S)-2-(3-chloro-phenoxymethyl)-pyrrolidine hydrochloride (Preparation 90, 430 mg, 2.0 mmol), hexacarbonylmolybdenum (50 mg, 0.2 mmol), palladium(II) acetate (4 mg, 0.02 mmol), and sodium carbonate (130 mg, 1.2 mmol) in water (0.82 mL, 45 mmol) was heated 20 min at 110° C. in the microwave. The reaction mixture was diluted with 1 N HCl and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was taken up in 1.2 mL of DMSO, filtered, and purified via HPLC (Prep: Phenomenex 250×30.0 mm 15 micron C18 column. 40 mL/min. Gradient 15% B to 100% B over 25 min. Solvent A: 7800 water/200 acetonitrile/8 TFA. Solvent B: 7200 acetonitrile/800 water/8 TFA).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741934B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-dc72073ce46d4fbc86ae40b01a14a287
Quellennotizuspto-grants-2014_06