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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048469Generated: October 30, 2026

Sodium → HCID 58573518, compound

https://huagongshe.com/reaction/1048469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
Reactant4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
Reactant(S)-2-((3S,5R,6S)-3-Allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-1-yl)butanalHCID 58573909—
CatalystAcetic AcidHCID 176—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 58573518HCID 58573518—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (S)-2-((3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-1-yl)butanal (84 mg, 0.189 mmol; Example 91, Step C), ethyl 4-aminobutyrate hydrochloride (127 mg, 0.756 mmol) and acetic acid (3 drops) in DCE/MeOH (3/1, 4.0 mL) was added sodium triacetoxyhydroborate (200 mg, 0.945 mmol) at 25° C. After being stirred at 25° C. for 18 h, the reaction was quenched by adding ice-cold saturated aqueous NaHCO3 solution and was extracted with DCM. The combined organic layers were washed (1×sat. aq. NaCl solution) and concentrated under reduced pressure. The residue was purified by reverse phase preparatory HPLC (acetonitrile in water with 0.1% TFA, gradient elution) to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-704a5d57b8364602abf157eded94b135
Source noteuspto-grants-2013_10