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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048397Generated: October 30, 2026

HCID 68000325, compound → HCID 67999636, compound

https://huagongshe.com/reaction/1048397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68000325HCID 68000325—
ReactantHCID 178418573HCID 178418573—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67999636HCID 67999636—

Reaction Steps

To a solution of (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-1-((S)-6-oxoheptan-3-yl)piperidin-2-one prepared above in Step C (78 mg, 0.16 mmol) in THF (1.6 mL) was added 1.4 M methylmagnesium bromide in toluene and THF (75:25) (344 μL, 0.481 mmol) at 0° C. Then the reaction was allowed to warm to rt and stirred for 2 h. The reaction was quenched (sat NH4Cl solution), extracted (2×EtOAc), and washed (sat. aq. NaCl solution). The combined organic layer was dried (Na2SO4) and concentrated under reduced pressure. Purification of the residue by chromatography on silica gel (12 g SiO2, 33% and 43% EtOAc/Hex) provided the title compound as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-857c5035d14a42b9bf3ab952c1d9cbfa
Source noteuspto-grants-2013_10