HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → HCID 18755775, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (Chlorothio)formyl chloride | HCID 75990 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18755775 | HCID 18755775 | — |
Reaction Steps
Another preferred embodiment involves the formation of yet another novel bifunctional compound (FIG. 5). Chlorocarbonyl sulfenyl chloride was reacted with 2mercaptoethanol and 2-mercaptopyridine. Ammonium carbonate solution was added to form 2-(2-Pyridinyl)dithio)ethanol as a colorless oil. Carbonyldiimidazole was added and the mixture was reacted with hydrazine to form 2-[(2-pyridinyl)dithio]ethyl hydrazinecarboxylate, compound 13. This compound was reacted with adriamycin hydrochloride and TFA and then acetonitrile to form the carboxylatehydrazone derivative of ADM (compound 4, FIG. 1) having a carboxylatehydrazone bond at the C-13 position of the ADM and having a reactive pyridinyldithio moiety.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05137877 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-e97eb0580a6046498f5f54613a808a8b |
| Source note | uspto-grants-1992_08 |