HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-nitrophenol → HCID 19012033, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-nitrophenol | HCID 6980 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 20061162 | HCID 20061162 | — |
| Reactant | HCID 20061251 | HCID 20061251 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19012033 | HCID 19012033 | — |
Reaction Steps
Preparation of 1,3-dimethyl-6-{4-[3-(4-chloro-2-nitrophenoxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione hydrochloride (Compound 140) ##STR125## 0.80 g of 4-chloro-2-nitrophenol, 1.13 g of 1,3-dimethyl-6-[4-(3-hydroxypropyl)piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione (Compound 139) and 1.21 g of triphenylphosphine were suspended in 15 ml of anhydrous tetrahydrofuran, followed by the addition of 0.80 g of diethyl azodicarboxylate. The resultant mixture was treated in a similar manner to Example 84-(2), thereby obtaining 1.43 g of 1,3-dimethyl-6-{4-[3-(4-chloro-2-nitrophenyloxy)propyl]piperazin-1-yl}-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-59e88b0b47d5428dba7802d5b09bf256 |
| Source note | uspto-grants-1991_04 |