HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 528831Erstellt: 26. Oktober 2026
Potassium Carbonate → 1-(2-(3,4-Dichlorophenyl)acetyl)indoline-5-sulfonamide
https://huagongshe.com/reaction/528831
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 3,4-Dichlorophenylacetic acid | HCID 79874 | — |
| Edukt | 2,3-dihydro-1H-indole-5-sulfonamide | HCID 8027252 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Sodium Bicarbonate | HCID 516892 | — |
| Produkt | 1-(2-(3,4-Dichlorophenyl)acetyl)indoline-5-sulfonamide | HCID 71061053 | 77% |
Reaktionsschritte
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)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09346795B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-a19deb8701c249ba909f1d5c7360479d |
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| Quellennotiz | uspto-grants-2016_05 |
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