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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12514Erstellt: 25. Oktober 2026

3-Chlorobenzenesulphonyl chloride → HCID 178464646, Verbindung

https://huagongshe.com/reaction/12514

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chlorobenzenesulphonyl chlorideHCID 17909—
EduktDiisopropylethylamineHCID 81531—
EduktHCID 178464603HCID 178464603—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178464646HCID 178464646—

Reaktionsschritte

6.39 g N-Ethyl-4,4-dimethyl-4,5-dihydro-pyrazole-1-carboxamidine hydrochloride was suspended in 65 mL DCM. 12.0 mL DIPEA and 3.96 mL 3-chloro-benzenesulfonyl chloride were added and the suspension was stirred for 20 h. at room temperature, resulting in a dark brown turbid solution. The mixture was extracted with 2M NaOH (2×125 mL) and 1M HCl (2×125 mL)7 washed with water (100 mL), and the organic layer was dried over Na2SO4 followed by evaporation under reduced pressure to yield 7.70 g of a brown oil. The oil (1.0 g) was dissolved in MTBE (3 mL) under reflux, and the solution was slowly cooled to room temperature, initializing crystallization The suspension was stirred for 10 min at room temperature, hexane (6 mL) was added over a period of 1 minute. The resulting suspension was stirred for 20 min. at room temperature and 50 min. at 0° C., and product was collected by filtration and washed with hexane (1 mL). Drying under reduced pressure at 40° C. yielded 0.85 g of a light-brown solid, m.p. 62-67° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728018B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-f74a5cfdc3c645d594fa518fd94b6452
Quellennotizuspto-grants-2010_06