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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423202Generated: November 1, 2026

(S)-1-(3-cyclobutoxy-4-methoxyphenyl)-3-(4-fluorobenzyl)piperazine → (S)-1-(4-(3-cyclobutoxy-4-methoxyphenyl)-2-(4-fluorobenzyl)piperazin-1-yl)-2-(1H-pyrazol-4-yl)ethanone

https://huagongshe.com/reaction/1423202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1-(3-cyclobutoxy-4-methoxyphenyl)-3-(4-fluorobenzyl)piperazineHCID 58189210—
Reactantmethyl 2-(1H-pyrazol-4-yl)acetateHCID 58189211—
Product(S)-1-(4-(3-cyclobutoxy-4-methoxyphenyl)-2-(4-fluorobenzyl)piperazin-1-yl)-2-(1H-pyrazol-4-yl)ethanoneHCID 5818920758%

Reaction Steps

Prepared by the method outlined for Example 275 using methyl 1H-pyrazol-4-ylacetate and (S)-1-(3-cyclobutoxy-4-methoxyphenyl)-3-(4-fluorobenzyl)piperazine as starting materials. Product was obtained as a colorless solid (58%). LC/MS 3.44 min, [M+1]+ 479.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927546B2
Source datasetuspto-grants-2015_01
ORD IDord-7a00bcb86d0d4275a16565fb94a36457
Source noteuspto-grants-2015_01