HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19598387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 14459520 | HCID 14459520 | — |
| Reactant | HCID 19598388 | HCID 19598388 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19598387 | HCID 19598387 | — |
Reaction Steps
0.11 g (1 mmol) of ethyl chloroformate is added, while stirring at -15° C., to a solution of 0.57 g (1 mmol) of N-(4-carboxyphenyl)-N-(4-toluenesulfonyl)acridine-9-carboxamide hydrobromide and 0.21 g (2 mmol) of triethylamine in 25 ml of anhydrous tetrahydrofuran. The mixture is stirred at the same temperature for 1 hour and then 0.12 9 (1 mmol) of N-hydroxysuccinimide is added. After a further hour, the mixture is left to stand at room temperature for 15 hours. It is evaporated in vacuo, the residue is taken up in ethyl acetate, and the solution is washed with water, sodium bicarbonate solution and water and dried over sodium sulfate. Evaporation yields 0.42 g (70.8% of theory) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783696 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-888bb95ca5a34fa7a1a515f44bcacb92 |
| Source note | uspto-grants-1998_07 |