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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262730Generated: November 3, 2026

Glycine → HCID 57513877, compound

https://huagongshe.com/reaction/2262730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
Reactant2-BromopyridineHCID 7973—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 57513875HCID 57513875—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57513877HCID 57513877—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1′-[2-(4-cyclobutylpiperazin-1-yl)-2-oxoethyl]spiro[indole-3,4′-piperidin]-2(1H)-one (0.052 mmol), 2-bromopyridine (0.078 mmol), CuI (2 mg, 0.01 mmol), K3PO4 (28 mg, 0.13 mmol), glycine (1 mg, 0.012 mmol) in 1,4-dioxane (3 ml) is degassed by Argon then heated in a sealed tube at 110° C. for 24 h. Solid is filtered and the filtrate is concentrated and purified by PTLC to give the title compound as a light yellow solid. LC-MS (M+1): 459.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851474B2
Source datasetuspto-grants-2010_12
ORD IDord-74fcd2bdc2214f748280201d41f6bba7
Source noteuspto-grants-2010_12