HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzenesulfonyl chloride, 3,4-dichloro- → 1-(3,4-Dichloro-benzenesulfonyl)-1H-indole-2-carboxylic acid methyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzenesulfonyl chloride, 3,4-dichloro- | HCID 7383 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Methyl 1H-indole-2-carboxylate | HCID 70992 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-(3,4-Dichloro-benzenesulfonyl)-1H-indole-2-carboxylic acid methyl ester | HCID 21705087 | 51% |
Reaktionsschritte
Methyl indole-2-carboxylate (0.15 g) was dissolved in DMF and sodium hydride (41 mg) was added in a single portion. The reaction was stirred for 1 hour, then 3,4-dichlorobenzenesulphonyl chloride (0.25 g) was added in a single portion. Stirring was continued for a further 2 hours and then the reaction was quenched by the addition of water. The reaction mixture was partitioned between water and ethyl acetate. Combined organic extracts were dried (MgSO4) and concentrated in vacuo and the residue purified by column chromatography using isohexane-5% ethyl acetate as eluent to give the desired end product as a solid (51%). NMR δ (CDCl3) 3.96 (s, 3H), 7.22-8.20 (m, 8H); M/z (+) 384 (MH+), 352, 175.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06288103B1 |
| Quelldatensatz | uspto-grants-2001_09 |
| ORD ID | ord-68781318143040b78dcc54e5d3867522 |
| Quellennotiz | uspto-grants-2001_09 |