HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiosemicarbazide → N-Ethyl-N-[3-(3-amino-1,2,4-triazolo[4,3-b]pyridazin-6-yl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Reactant | N-Ethyl-N-[3-(6-chloro-3-pyridazinyl)phenyl]acetamide | HCID 14280297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Ethyl-N-[3-(3-amino-1,2,4-triazolo[4,3-b]pyridazin-6-yl)phenyl]acetamide | HCID 15595669 | — |
Reaction Steps
A solution of 2.0 g of N-ethyl-N-[3-(6-chloro-3pyridazinyl)phenyl]acetamide and 1.32 g of thiosemicarbazide in 100 ml of ethanol was refluxed for 8 hours, then evaporated in vacuo. To the residue was added 100 ml of glacial acetic acid. This mixture was refluxed overnight, then the solvent was removed in vacuo, 150 ml of water added and aqueous sodium bicarbonate added to neutralize the solution. This mixture was extracted with dichloromethane:methanol (9:1). The extracts were dried and evaporated. The residue was chromatographed on a silica gel column eluting with dichloromethane:methanol (9:1). The fractions containing product were combined and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892873 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-86d1ab1d9cd24198898346a4b1fc3433 |
| Source note | uspto-grants-1990_01 |