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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048521Generated: October 28, 2026

HCID 58573190, compound → HCID 58573990, compound

https://huagongshe.com/reaction/1048521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58573190HCID 58573190—
ReactantHCID 178418573HCID 178418573—
ProductHCID 58573990HCID 58573990—

Reaction Steps

By the procedure of Example 149, Step A, (S)-2-((3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-1-yl)-2-cyclopropylacetaldehyde (Example 257, Step C, 866 mg, 1.897 mmol) was treated with methyl magnesium bromide to give the diastereomeric alcohols (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((1S,2R)-1-cyclopropyl-2-hydroxypropyl)-3-methylpiperidin-2-one and (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((1S,2S)-1-cyclopropyl-2-hydroxypropyl)-3-methylpiperidin-2-one as a white foam. MS (ESI) m/z=472 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-4378d3f9eae64f4f8c1d11e11f0ae0b2
Source noteuspto-grants-2013_10