HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 20061223, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Methoxy-5-nitrophenol | HCID 69471 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 20061251 | HCID 20061251 | — |
| Reactant | HCID 20061272 | HCID 20061272 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20061223 | HCID 20061223 | — |
Reaction Steps
Preparation of 1,3-dimethyl-6-{4-[3-(2-methoxy-5-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione hydrochloride (Compound 160) ##STR141## 0.9 g of 2-methoxy-5-nitrophenol, 1.0 g of 1,3-dimethyl-6-[4-(3-hydroxypropyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione (Compound 139) and 1.1 g of triphenylphosphine were suspended in 20 ml of anhydrous tetrahydrofuran, followed by the addition of 0.67 ml of diethyl azodicarboxylate. The thus-prepared mixture was treated in a similar manner to Example 84-(2), thereby obtaining 1.2 g of 1,3-dimethyl-6-{4-[3-(2-methoxy-5-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008267 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-cdb11c3ce3ed4b41acf5f470d5151a7e |
| Source note | uspto-grants-1991_04 |