HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → (S)-tert-Butyl (1-(4-(imidazo[1,2-b]pyridazin-6-yl)piperazin-1-yl)-4-methyl-1-oxopentan-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 6-Fluoroimidazo[1,2-b]pyridazine | HCID 15144436 | — |
| Reactant | 1,1-dimethylethyl [(1S)-3-methyl-1-(1-piperazinylcarbonyl)butyl]carbamate | HCID 59868341 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-tert-Butyl (1-(4-(imidazo[1,2-b]pyridazin-6-yl)piperazin-1-yl)-4-methyl-1-oxopentan-2-yl)carbamate | HCID 86696490 | 78% |
Reaction Steps
To 305 mg (2.23 mmol) of 6-fluoroimidazo[1,2-b]pyridazine, was added 1.00 g (3.34 mmol) of (S)-tert-butyl(4-methyl-1-oxo-1-(piperazin-1-yl)pentan-2-yl)carbamate, 10 mL of isopropyl alcohol, and 0.93 mL (6.68 mmol) of TEA. This was microwaved at 150° C. for 0.5 hr. It was diluted with EtOAc, washed with brine, and the organic layer was dried over MgSO4, and then concentrated. It was purified on the ISCO with a 40 gram column eluting with 0-10% MeOH/DCM to obtain the desired product in 78% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969565B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-ccc26de0eb2f40a8b45e8dd4080c18ef |
| Source note | uspto-grants-2015_03 |