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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301766Generated: October 31, 2026

Benzoyl chloride → HCID 70157733, compound

https://huagongshe.com/reaction/2301766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 70157605HCID 70157605—
ProductHCID 70157733HCID 70157733—

Reaction Steps

Using essentially the same procedure as Example 16, Step A and B, 1-(RS)-((t-butoxycarbonyl)amino)-3-(SR)-((4-(N-(4-nitrobenzylaminocarbonyl)-N-(allyl)amino)piperidin-1-yl)methyl)-4-(SR)-phenylcyclopentane from Example 22 (derived from the lower isomer from Example 20, Step E) was deblocked and acylated with benzoyl chloride to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-68d76f3eeca54930bff8bb6ec0726e81
Source noteuspto-grants-2002_12