HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-(4-aMino-3-Methoxyphenyl)piperazin-1-yl)ethanone → HCID 72546716, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-(4-aMino-3-Methoxyphenyl)piperazin-1-yl)ethanone | HCID 55232737 | — |
| Reactant | HCID 118105738 | HCID 118105738 | — |
| Solvent | HCID 19698338 | HCID 19698338 | — |
| Product | HCID 72546716 | HCID 72546716 | — |
Reaction Steps
1-(4-(4-amino-3-methoxyphenyl)piperazin-1-yl)ethanone (40 mg) prepared in Preparation Example 1 and 1-(4-(4-(2,5-dichloropyrimidine-4-ylamino)-3-ethoxyphenyl)piperazin-1-yl)ethanone (50 mg) prepared in Preparation Example 15 were dissolved in 0.08M HCl ethoxyethanol solution (1.2 mL), and allowed to react at 115° C. overnight. Upon completion of the reaction, the solvent of the mixture was removed under reduced pressure, diluted with ethyl acetate, neutralized with an aqueous saturated sodium carbonate solution, water was removed from the organic layer with sodium sulfate, and the solvent was removed under reduced pressure. The mixture was purified by column chromatography to obtain a target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199944B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-38dfc35b5e5d4bbeacce2517d28a0079 |
| Source note | uspto-grants-2015_12 |