HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → (+/-)-cis-8,9-Dimethoxy-6-[4-bis(p-toluenesulfonyl)aminophenyl]-1,2,3,4,4a,10b-hexahydrophenanthridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (+/-)-cis-8,9-Dimethoxy-6-(4-p-toluenesulfonamidophenyl)-1,2,3,4,4a,10b-hexahydrophenanthridine | HCID 15410435 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (+/-)-cis-8,9-Dimethoxy-6-[4-bis(p-toluenesulfonyl)aminophenyl]-1,2,3,4,4a,10b-hexahydrophenanthridine | HCID 86755880 | — |
Reaction Steps
2.0 g of (+/-)-cis-8,9-dimethoxy-6-(4-p-toluenesulfonamidophenyl)-1,2,3,4,4a,10b-hexahydrophenanthridine in 5 ml of dimethylformamide and then 1.0 g of p-toluenesulfonyl chloride in 5 ml of dimethylformamide are added dropwise to a suspension of 200 mg of 80% strength sodium hydride in 20 ml of dimethylformamide. After stirring at RT for 2 h, the mixture is added to ice-water and extracted with ethyl acetate/diethyl ether in the ratio 1:1. After drying and concentration of the organic phase, the residue is chromatographed on silica gel using a mixture of ethyl acetate/petroleum ether in the ratio 4:1. After concentration of the corresponding eluate fractions, the title compound of m.p. 120-130° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127378 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-5b08debcd55a4418b958727c376df586 |
| Source note | uspto-grants-2000_10 |