HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 68140870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 68139588 | HCID 68139588 | — |
| Reactant | HCID 68139760 | HCID 68139760 | — |
| Product | HCID 68140870 | HCID 68140870 | — |
Reaction Steps
Oily 1-N-phenylpiperazinocarbonylethyl-3-phenyl-5-methylindazole (4.0 g) which had been prepared by reacting in order 1-hydroxycarbonylethyl-3-phenyl-5-methylindazole with ethyl chlorocarbonate and N-phenyl-piperazine was treated with the use of lithium aluminum hydride (1.2 g) by the procedure similar to that described in Example 27 to obtain 6.1 g of 1-N-phenylpiperazino-propyl-3-phenyl-5-methylindazole hydrochloride having a melting point between 195°-200° C after recrystallization from ethanol-ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994890 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-3ed3288bb27542d2b399cca86d3aa19e |
| Source note | uspto-grants-1976_11 |