HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 20061254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 20061251 | HCID 20061251 | — |
| Reactant | HCID 20061337 | HCID 20061337 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20061254 | HCID 20061254 | 79.4% |
Reaction Steps
0.7 g of 2-benzylamino-4-nitrophenol, 0.8 g of 1,3-dimethyl-6-[4-(3-hydroxypropyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione (Compound 139) and 0.9 g of triphenylphosphine were suspended in 20 ml of anhydrous tetrahydrofuran, followed by the addition of 0.65 g of diethyl azodicarboxylate. The thus-prepared mixture was treated in a similar manner to Example 84-(2), thereby obtaining 0.93 g of 1,3-dimethyl-6-{4-[3-(2-benzylamino-4-nitrophenyloxy)propyl]piperazin-1yl}-2,4(1H,3H)-pyrimidinedione as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008267 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-dcb30a4711e2425fa2f0c9b165eb92f2 |
| Source note | uspto-grants-1991_04 |