Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 528823Erstellt: 26. Oktober 2026

Potassium Carbonate → 1-(Cyclohexanecarbonyl)indoline-5-sulfonamide

https://huagongshe.com/reaction/528823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktCyclohexanecarbonyl chlorideHCID 75938—
Edukt2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 6069874220,1%

Reaktionsschritte

To a solution of indoline-5-sulfonamide (Intermediate 54A, 100 mg, 0.50 mmol) in MeCN (5.0 mL) was added cyclohexanecarbonyl chloride (0.14 mL, 1.00 mmol) and K2CO3 (174 mg, 1.26 mmol). The resulting reaction mixture was stirred at room temperature overnight and then diluted with EtOAc and sat. aq. NaHCO3 solution. The organic layer was washed with 1 N aq. NaOH solution, followed by 10% aq. LiCl solution. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo. The residue was triturated with CH2Cl2 to give the title compound (31 mg, 20%) as a white solid. 1H NMR (DMSO-d6) δ 8.16 (d, J=6.8 Hz, 1H), 7.64-7.60 (m, 2H), 7.19 (m, 2H), 4.22 (t, J=8.5 Hz, 2H), 3.21-3.16 (m, 2H), 2.62-2.55 (m, 1H), 1.91-1.65 (m, 5H), 1.45-1.16 (m, 5H); MS(ESI+) m/z 309.1 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346795B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-1a274eb274754d368c893024268328f8
Quellennotizuspto-grants-2016_05