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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375005Generated: October 29, 2026

HCID 57210497, compound → HCID 86602695, compound

https://huagongshe.com/reaction/1375005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57210497HCID 57210497—
CatalystLindlars catalystHCID 131709914—
SolventMethanolHCID 887—
ProductHCID 86602695HCID 8660269566.5%

Reaction Steps

A solution of (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3-hydroxy-4-methylbenzyl)-4-[4-[(2S)-2-(methoxymethyl)-morpholino]-2-butynyl]piperazine (0.33 g) in methanol (10 ml) was hydrogenated over Lindlar catalyst (63 mg). After removal of catalyst by filtration, the filtrate was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using methanol/dichloromethane (1:9) as an eluent. The fractions containing the objective compound were collected and evaporated in vacuo to give (2R)-1-[3,5-bis(trifluoromethyl)-benzoyl]-2-(3-hydroxy-4-methylbenzyl)-4-[(Z)-4-[(2S)-2-(methoxymethyl)morpholino]-2-butenyl]piperazine (0.22 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166598B2
Source datasetuspto-grants-2007_01
ORD IDord-db22c19c802c47d3a61dfbfdfc0b5c79
Source noteuspto-grants-2007_01