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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730945Generated: October 31, 2026

1-Phenylpiperazine → HCID 68140870, compound

https://huagongshe.com/reaction/1730945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantEthyl chloroformateHCID 10928—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 68139588HCID 68139588—
ReactantHCID 68139760HCID 68139760—
ProductHCID 68140870HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994890
Source datasetuspto-grants-1976_11
ORD IDord-3ed3288bb27542d2b399cca86d3aa19e
Source noteuspto-grants-1976_11