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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411671Generated: November 1, 2026

(S)-5-(Hydroxymethyl)-2-pyrrolidinone → (S)-1-{4-[4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazine-1-carbonyl]-3-methanesulfonylphenyl}-5-hydroxymethylpyrrolidin-2-one

https://huagongshe.com/reaction/2411671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-5-(Hydroxymethyl)-2-pyrrolidinoneHCID 643511—
Reactant(4-Bromo-2-methanesulfonylphenyl)[4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl]methanoneHCID 58484821—
Product(S)-1-{4-[4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazine-1-carbonyl]-3-methanesulfonylphenyl}-5-hydroxymethylpyrrolidin-2-oneHCID 7125227956.8%

Reaction Steps

Using (S)-5-hydroxymethylpyrrolidin-2-one (127 mg) and (4-bromo-2-methanesulfonylphenyl)[4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl]methanone (478 mg) described in Preparation Example 126 and by the reaction and treatment in the same manner as in Example 1, the title compound (291 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-89ec653f905642b08d1b0a31e674c933
Source noteuspto-grants-2014_08