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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239331Erstellt: 24. Oktober 2026

Morpholine-4-sulfonyl chloride → HCID 57990006, Verbindung

https://huagongshe.com/de/reaction/239331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholine-4-sulfonyl chlorideHCID 12798265—
Edukt3-[5-(2-Chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]anilineHCID 57990046—
LösungsmittelPyridineHCID 1049—
ProduktHCID 57990006HCID 5799000613,8%

Reaktionsschritte

To a solution of 3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]aniline (1.5 g, 4.5 mmol) in pyridine (15 mL) was added morpholine-4-sulfonyl chloride (1.26 g, 6.8 mmol). The reaction was stirred at rt for 12 h. Then the reaction was washed with water (50 mL), and extracted with DCM (2×50 mL). The organic layer was washed with brine, dried over anhydrous NaSO4, filtrated and concentrated under reduced pressure to give the crude product, which was purified by column chromatography on silica gel (DCM:EtOAc 60:1) to afford the title compound of Step A (297 mg, 13.8% yield). 1H NMR (400 MHz, CDCl3) δ ppm 8.30 (d, J=5.3 Hz, 1H), 7.27-7.36 (m, 2H), 7.21-7.26 (m, 2H), 6.98 (d, J=5.3 Hz, 1H), 3.58-3.64 (m, 4H), 3.22-3.33 (m, 1H), 3.14-3.21 (m, 4H), 1.40 (d, J=7.0 Hz, 6H). MS (ES+): 480 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642759B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-d3f49aefe1374d90a27c3e5cdf488802
Quellennotizuspto-grants-2014_02