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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656654Generated: November 2, 2026

1-[2-(2-Hydroxyethoxy)ethyl]piperazine → HCID 57664407, compound

https://huagongshe.com/reaction/656654

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-(2-Hydroxyethoxy)ethyl]piperazineHCID 139436—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant3-Amino-5-chloro-6-methanesulfinyl-4-methyl-thieno[2,3-b]pyridine-2-carboxylic acid cyclopropylamideHCID 57664420—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57664407HCID 5766440717.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-[2-(2-hydroxyethoxy)ethyl]piperazine (1.061 g, 6.09 mmol) in THF (3 ml) at room temperature is added dropwise a solution of lithium bis(trimethylsilyl) amide (1.0 M in hexanes)(3.50 ml, 3.50 mmol). The reaction mixture is stirred for 15 minutes and then is treated with 3-amino-5-chloro-6-methanesulfinyl-4-methyl-thieno[2,3-b]pyridine-2-carboxylic acid cyclopropylamide (0.345 g, 1.00 mmol). The reaction mixture is heated at 80° C. in a sealed tube for 1.5 hours, cooled to room temperature, and then quenched by the addition of water (15 ml). Ice is added to the reaction mixture and, while stirring, a yellow precipitate forms. This solid is collected by filtration and placed in the vacuum oven to dry (60° C. for 16 hours). This affords the title compound as a yellow solid (0.078 g, 17%). Mass (m/z): 454.2 (M++1), 452.2 (M+−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071776B2
Source datasetuspto-grants-2011_12
ORD IDord-02c419dc4fcd4250b5c3dbc0fe1de345
Source noteuspto-grants-2011_12