HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → HCID 15289639, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 15289638 | HCID 15289638 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15289639 | HCID 15289639 | — |
Reaction Steps
A solution of 540 mg of 3-methylsulfonyl-4-(1,6-dihydro-6-oxo-3-pyridazinyloxy)benzoic acid [obtainable by reacting 3-methylsulfonyl-4-chlorobenzoic acid with 3-trimethylsilyl-oxy-6-oxo-1,6-dihydropyridazine] and 300 mg of carbonyldiimidazole in 15 ml of THF is stirred at room temperature for 2 hours, and 383 mg of guanidine are then added to it. This mixture is then stirred for a further two hours. After the customary working-up, N-diaminomethylene-3-methylsulfonyl-4-(1,6-dihydro-6-oxo-3-pyridazinyloxy)benzamide is obtained, m.p. 268-270°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06022883 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-0ebbee2040f54acf9dc814748fecb0ce |
| Source note | uspto-grants-2000_02 |