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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 528831생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/528831

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Oxalyl chlorideHCID 65578—
반응물3,4-Dichlorophenylacetic acidHCID 79874—
반응물2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
촉매DimethylformamideHCID 6228—
용매1,2-DichloroethaneHCID 11—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
생성물1-(2-(3,4-Dichlorophenyl)acetyl)indoline-5-sulfonamideHCID 7106105377%

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346795B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-a19deb8701c249ba909f1d5c7360479d
출처 메모uspto-grants-2016_05