HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine → (R)-3-Benzyl-4,5-dimethyl-6-(3-methylpiperazin-1-yl)pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine | HCID 59191518 | — |
| Reactant | HCID 178419772 | HCID 178419772 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | (R)-3-Benzyl-4,5-dimethyl-6-(3-methylpiperazin-1-yl)pyridazine | HCID 59191647 | 66% |
Reaction Steps
3-Chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine (400 mg, 1.66 mmol, 1 eq) is added to a solution of benzylzinc bromide (12.3 mL 0.5 M in THF, 6.64 mmol, 4 eq) and tetrakis(triphenylphosphine)palladium (100 mg, 0.08 mmol, 0.05 eq) in a microwave vial. The vial is sealed and irradiated in the microwave at 100° C. (high absorption setting) for 40 min. The reaction mixture is concentrated and purified by silica gel chromatography (5-20% EtOAc/heptane) to yield the desired compound (324 mg, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409871B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-b85ee086af1d4a0090f7dcb68b855650 |
| Source note | uspto-grants-2016_08 |