HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → HCID 23153692, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Hydrazinecarboxaldehyde | HCID 12229 | — |
| Reactant | HCID 23153698 | HCID 23153698 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23153692 | HCID 23153692 | 75.2% |
Reaction Steps
240 mg (4.0 mmol) of formohydrazide and 551 mg (4.0 mmol) of triethylamine hydrochloride were added to a xylene solution (10 ml) of 543 mg (2.0 mmol) of 4-chloro-1-(4-methoxyphenyl)-pyrido[3,4-d]pyridazine, and then stirred under reflux for 2 hours. Water was added to the reaction liquid, extracted with chloroform, and the organic layer was washed with saturated saline water. This was dried with anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain 417 mg of a crude product of 6-(4-methoxyphenyl)-pyrido[3,4-d][1,2,4]triazolo[4,3-b]pyridazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645756B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-b657e60f1eb74a29826d442bd8ff3a2a |
| Source note | uspto-grants-2010_01 |