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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063123Generated: November 2, 2026

1-Benzylpiperazine → HCID 10429053, compound

https://huagongshe.com/reaction/1063123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
ReactantHCID 23401030HCID 23401030—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10429053HCID 10429053—

Reaction Steps

A mixture of 20 mg trifluoromethanesulfonic acid 3-amino-2-carbamoyl-thieno[2,3-b]pyridin-4-yl ester and 50 microL of N-benzylpiperazine in 1 mL of dry dioxane was purged with N2 and capped and left at room temperature overnight. The reaction was diluted with EtOAc, washed four times with water, dried and concentrated to dryness in vacuo. The product was purified on a 2 mm silica gel prep plate, developing and eluting the band with MeOH—CH2Cl2 mixtures and then concentrating to dryness. The product was re-dissolved in 5-10% MeOH—CH2Cl2, filtered to remove silica gel, concentrated, and dried in vacuo at 60° C. overnight to provide 7.9 mg of the title compound as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964956B2
Source datasetuspto-grants-2005_11
ORD IDord-7c082d2d1f144ae2a2a43d235eef4ba0
Source noteuspto-grants-2005_11