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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500152Generated: October 30, 2026

Tert-butyl 2-[4-(2-aminopyrimidin-5-yl)-2-fluorophenoxy]propionate → Tert-butyl 2-[2-fluoro-4-[3-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-a]pyrimidin-6-yl]phenoxy]propanoate

https://huagongshe.com/reaction/500152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-[4-(2-aminopyrimidin-5-yl)-2-fluorophenoxy]propionateHCID 67223953—
ReactantChloro(1-quinolin-6-ylcyclopropyl)acetaldehydeHCID 86621504—
SolventIsopropanolHCID 3776—
ProductTert-butyl 2-[2-fluoro-4-[3-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-a]pyrimidin-6-yl]phenoxy]propanoateHCID 6846301142%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 2-[4-(2-aminopyrimidin-5-yl)-2-fluorophenoxy]propanoate (0.33 g, 1.0 mmol) and chloro(1-quinolin-6-ylcyclopropyl)acetaldehyde (0.24 g, 1.0 mmol) in isopropanol was heated at 100° C. overnight. After cooling to RT, the mixture was purified by RP-HPLC (pH 2.0) to afford the desired product (0.22 g, 42%). LCMS: (M+H)=525.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-63b40e46fb164095b0e597f6485391c2
Source noteuspto-grants-2010_08