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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411662Generated: November 4, 2026

(R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone → HCID 71252271, compound

https://huagongshe.com/reaction/2411662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinoneHCID 7128291—
Reactant(4-Bromo-2-methanesulfonylphenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanoneHCID 58484505—
ProductHCID 71252271HCID 7125227142.5%

Reaction Steps

Using (R)-5-hydroxymethylpyrrolidin-2-one (409 mg) and (4-bromo-2-methanesulfonylphenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone (1.53 g) described in Preparation Example 112 and by the reaction and treatment in the same manner as in Example 1, (R)-1-{4-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]-3-methanesulfonylphenyl}-5-hydroxymethylpyrrolidin-2-one (700 mg) was obtained. Using the obtained (R)-1-{4-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]-3-methanesulfonylphenyl}-5-hydroxymethylpyrrolidin-2-one (700 mg) and methyl tosylate (0.21 mL) and by the reaction and treatment in the same manner as in Example 36, the title compound (319 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-64904900a71d4bf188312f9ab16881b2
Source noteuspto-grants-2014_08