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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301767Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 70156382, compound

https://huagongshe.com/reaction/2301767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 70157605HCID 70157605—
ProductHCID 70156382HCID 70156382—

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, Step H (derived from the lower isomer from Example 20, Step E) was deblocked and acylated with phenylsulfonyl chloride to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-0cf980ef50674c84bb5b89615dd8a8a2
Source noteuspto-grants-2002_12