HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 6-(1-Anthraquinonecarbonyl)-3,6,10,16-tetraazabicyclo-[10.3.1]hexadeca-1(16),12,14-triene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-(1-Anthraquinonecarbonyl)-3,10-bis (2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicylo[10.3.1]hexadeca-1(16),12,14-triene | HCID 21257333 | — |
| Product | 6-(1-Anthraquinonecarbonyl)-3,6,10,16-tetraazabicyclo-[10.3.1]hexadeca-1(16),12,14-triene | HCID 54533106 | 80% |
Reaction Steps
The title compound was prepared following the procedures illustrated above in Example 78 using 6-(1-anthraquinonecarbonyl)-3,10-bis(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1(16),12,14-triene (1.02 g, 1.24 mmol), thiophenol (0.41 g, 3.72 mmol) and K2CO3 (1.7 g, 12.5 mmol). The crude material was purified by flash chromatography on a silica gel column using CH2Cl2 and then MeOH, 15:1 MeOH—NH4OH (30%) as eluents to give 0.45 g (80%) of the title compound as a pale yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191273B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-5934d6d71a1543e391f880063694f60b |
| Source note | uspto-grants-2001_02 |