Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433093Generated: November 2, 2026

Ethanolamine → 4-(6-Chloro-benzo[b]thiophene-2-sulfonyl)-1-{1-[2-(2-hydroxy-ethylamino)-pyrimidin-4-yl]-piperidin-4-ylmethyl}-piperazin-2-one

https://huagongshe.com/reaction/1433093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant4-(6-Chloro-benzo[b]thiophene-2-sulfonyl)-1-[1-(2-chloro-pyrimidin-4-yl)-piperidin-4-ylmethyl]-piperazin-2-oneHCID 9807308—
SolventEthanolHCID 702—
Product4-(6-Chloro-benzo[b]thiophene-2-sulfonyl)-1-{1-[2-(2-hydroxy-ethylamino)-pyrimidin-4-yl]-piperidin-4-ylmethyl}-piperazin-2-oneHCID 67013858—

Reaction Steps

To a solution of 4-(6-chloro-benzo[b]thiophene-2-sulfonyl)-1-[1-(2-chloro-pyrimidin-4-yl)-piperidin-4-ylmethyl]-piperazin-2-one (0.40 g, 0.74 mmol) in EtOH is added ethanolamine (0.089 mL, 1.5 mmol). The solution is heated to reflux for 18 h and evaporated to dryness. The residue is chromatographed eluting successively with 1%, 2% and 4% MeOH in CH2Cl2. Fractions containing only product are combined and the solvent evaporated. Trituration with ether afforded the title compound as a yellow solid: MS (ESI): m/z 565 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-9b2b5a9323014e1ba0b15686aa0b7cfb
Source noteuspto-grants-2009_11