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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257925Generated: November 2, 2026

1-[2-Chloro-1-hydroxy-2-(1-quinolin-6-ylcyclopropyl)ethyl]pyrrolidine-2,5-dione → tert-butyl 3-[3-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-a]pyrimidin-6-yl]-1H-pyrazol-1-ylacetate

https://huagongshe.com/reaction/1257925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-Chloro-1-hydroxy-2-(1-quinolin-6-ylcyclopropyl)ethyl]pyrrolidine-2,5-dioneHCID 67223833—
Reactanttert-butyl[3-(2-aminopyrimidin-5-yl)-1H-pyrazol-1-yl]acetateHCID 90849675—
SolventEthanolHCID 702—
Producttert-butyl 3-[3-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-a]pyrimidin-6-yl]-1H-pyrazol-1-ylacetateHCID 6722471137%

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of tert-butyl[3-(2-aminopyrimidin-5-yl)-1H-pyrazol-1-yl]acetate (16 mg, 0.058 mmol) and 1-[2-chloro-1-hydroxy-2-(1-quinolin-6-ylcyclopropyl)ethyl]pyrrolidine-2,5-dione (20 mg, 0.058 mmol) in ethanol (0.3 mL) was stirred overnight at 105° C. The reaction mixture was purified by RP-HPLC (pH 10) to afford the desired product (10 mg, 37%). LCMS: (M+H)=467.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-f37c97dc5aa443aa803335cb223789c7
Source noteuspto-grants-2013_06