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HRID 528831作成日:2026年10月27日

Potassium Carbonate → 1-(2-(3,4-Dichlorophenyl)acetyl)indoline-5-sulfonamide

https://huagongshe.com/reaction/528831

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Oxalyl chlorideHCID 65578—
反応物3,4-Dichlorophenylacetic acidHCID 79874—
反応物2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
触媒DimethylformamideHCID 6228—
溶媒1,2-DichloroethaneHCID 11—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BicarbonateHCID 516892—
生成物1-(2-(3,4-Dichlorophenyl)acetyl)indoline-5-sulfonamideHCID 7106105377%

反応手順

To a suspension of 2-(3,4-dichlorophenyl)acetic acid (137 mg, 0.67 mmol) in DCE (2.0 mL) was added oxalyl chloride (908 μL, 1.82 mmol, 2.0M solution in CH2Cl2) (0.908 mL, 1.816 mmol) followed by one drop of DMF. The resulting reaction mixture was stirred at room temperature for 40 min and then concentrated in vacuo. To a solution of the crude residue in MeCN (4.0 mL) was added indoline-5-sulfonamide (120 mg, 0.61 mmol) and K2CO3 (167 mg, 1.21 mmol). The reaction mixture was stirred at room temperature for 1 h. Additional indoline-5-sulfonamide (40 mg, 0.20 mmol) was added, and the reaction mixture was allowed to stir at room temperature overnight. The reaction mixture was then diluted with EtOAc and sat. aq. NaHCO3 solution. The organic layer was washed with 10% aq. LiCl solution and then dried over MgSO4, filtered and concentrated in vacuo. The residue was triturated with CH2Cl2 to give the title compound (180 mg, 77%) as a pale yellow solid. 1H NMR (DMSO-d6) δ 8.11 (d, J=8.4 Hz, 1H), 7.59 (m, 4H), 7.29 (dd, J=8.1, 2.0 Hz, 1H), 7.22 (s, 2H), 4.26 (t, J=8.5 Hz, 2H), 3.94 (s, 2H), 3.24 (t, J=8.5 Hz, 2H); MS(ESI+) m/z 385.0 (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-a19deb8701c249ba909f1d5c7360479d
出典メモuspto-grants-2016_05