HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Mirtazapine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol | HCID 10221435 | — |
| Product | Mirtazapine | HCID 4205 | 95% |
Reaction Steps
1-(3-Hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine (1.8 g) is added to ˜5 mL of concentrated sulfuric acid. The resulting solution is mixed at 350° C. for 6 hours. After cooling, the reaction mixture is added to 25 g of ice under mixing and basified with a concentrated ammonia solution or sodium hydroxide solution to pH=10. The separated precipitate is extracted into methylene chloride and the extract is evaporated to dryness; 1.6 g of Mirtazapine is obtained (yield 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576764B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-77349d81ba8442899937127503f714bc |
| Source note | uspto-grants-2003_06 |