HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13258487, compound → HCID 13469150, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13258487 | HCID 13258487 | — |
| Reactant | HCID 20226916 | HCID 20226916 | — |
| Reactant | HCID 20226919 | HCID 20226919 | — |
| Product | HCID 13469150 | HCID 13469150 | — |
Reaction Steps
The above-named compound is prepared in the same manner as described for the aminopyridazines of Example 38, excepting that 3-chloro-4-methyl-6-(2-thienyl)pyridazine is substituted for 3-chloro-4,5-dimethyl-6-phenylpyridazine. The product obtained has a melting point of 50°-52° C. 3-(Dimethylamino)-4-methyl-6-(3-thienyl)pyridazine, a red oil, (Example 51a) is made in the same manner as described above for the 2-thienyl derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04623376 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-80acaf92a7384ca3afa3f2ccc0cc0e5a |
| Source note | uspto-grants-1986_11 |