HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-Isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanone, dihydrochloride monohydrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | (4-Isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanone | HCID 10042344 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-Isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanone, dihydrochloride monohydrate | HCID 131728157 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of (4-isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanone (2.0 g, 6.0 mmol) in absolute EtOH (20 mL) was treated with HCl(g) (0.5 g, 13.7 mmol) at room temperature. The resulting suspension was stirred for 1 h, and then MTBE (5 mL) was added. The suspension was cooled to 0° C. and filtered. The filter cake was washed with MTBE (20 mL), and the solid was dried in a vacuum oven at 60° C. for 20 h to yield crude title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063206B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-cc345ac0f92648af85388d452b0d69a8 |
| Source note | uspto-grants-2011_11 |