HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646877Generated: October 31, 2026
Methyl Ethyl Ketone → HCID 14726867, compound
https://huagongshe.com/reaction/1646877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 11724258 | HCID 11724258 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14726867 | HCID 14726867 | — |
Reaction Steps
0.9 g (24 mmol) of sodium borohydride is added to a suspension of 2.8 g (12 mmol) of nickel dichloride hexahydrate in a solution, cooled to 0° C., of 2 g (6 mmol) of 4-nitro-1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-pyrazole, Example 7, and 10 ml of methyl ethyl ketone in 50 ml of ethanol. This temperature of 0° C. is maintained for 30 minutes, the mixture is allowed to rise to room temperature, stirring is continued for 2 hours, the mixture is evaporated under vacuum, the residue is taken up with ethyl acetate and 1.22 g of 4-(2-butylamino)1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-pyrazole are obtained in liquid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05182281 |
|---|
| Source dataset | uspto-grants-1993_01 |
|---|
| ORD ID | ord-252c78fe7b9a40c3bb246fa6701a959e |
|---|
| Source note | uspto-grants-1993_01 |
|---|