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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646918Generated: November 1, 2026

1-Benzyl-4-[10-(2-tetrahydropyranyloxy)decyl]piperazine → HCID 19021618, compound

https://huagongshe.com/reaction/1646918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-[10-(2-tetrahydropyranyloxy)decyl]piperazineHCID 19021614—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 19021618HCID 1902161882%

Reaction Steps

A 583 mg (1.40 mmoles) quantity of 1-benzyl-4-[10-(2-tetrahydropyranyloxy)decyl]piperazine was dissolved in 20 ml of ethanol, and 200 mg of 10% palladium-carbon was added thereto and the mixture was shaken at 3 atm. for 8 hours under a hydrogen atmosphere. The catalyst was filtered off and the filtrate was evaporated to dryness, giving 375 mg (yield: 82%) of N-[10-(2-tetrahydropyranyloxy)decyl]piperazine. Then, using N-t-butoxycarbonylphenylglycine and N-[10-(2-tetrahydropyranyloxy)decyl]piperazine, 1-(2-amino-2-phenylacetyl)-4-[10-(2-tetrahydropyranyloxy)decyl]piperazine was prepared in the same manner as in Reference Example 1. The obtained product was treated by the same procedure as in Reference Example 3, giving 384 mg (yield: 75%) of 1-(2-amino-2-phenylethyl) -4-[10-(2tetrahydropyranyloxy)decyl]piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182284
Source datasetuspto-grants-1993_01
ORD IDord-fd328f5ca30c472fa363f2802a484f57
Source noteuspto-grants-1993_01