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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646440Generated: October 30, 2026

(5-Bromothiophen-2-yl)(piperidin-1-yl)methanone → [2-(S)-(2-(R)-methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-{4-[5-(piperidine-1-carbonyl)-thiophen-2-yl]-phenyl}-methanone

https://huagongshe.com/reaction/646440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Bromothiophen-2-yl)(piperidin-1-yl)methanoneHCID 25236221—
Reactant[2-(S)-(2-(R)-Methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanoneHCID 57980025—
Product[2-(S)-(2-(R)-methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-{4-[5-(piperidine-1-carbonyl)-thiophen-2-yl]-phenyl}-methanoneHCID 1160512048%

Reaction Steps

The title compound is prepared in a manner substantially analogous to General Procedure A using [2-(S)-(2-(R)-methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanone (550 mg, 1.4 mmol) and (5-Bromo-thiophen-2-yl)-piperidin-1-yl-methanone (CAS 626242-11-3) (315 mg, 1.2 mmol) to give 260 mg (48% yield). MS (ES+) 466.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705025B2
Source datasetuspto-grants-2010_04
ORD IDord-d50ba011e3e543fc8b45db885f1835be
Source noteuspto-grants-2010_04