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HRID 528823作成日:2026年10月27日

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

https://huagongshe.com/reaction/528823

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Cyclohexanecarbonyl chlorideHCID 75938—
反応物2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BicarbonateHCID 516892—
生成物1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 6069874220.1%

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346795B2
出典データセットuspto-grants-2016_05
ORD IDord-1a274eb274754d368c893024268328f8
出典メモuspto-grants-2016_05