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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657269Generated: October 28, 2026

Ethylene Glycol → 4-[7-(2-Hydroxy-ethoxy)-quinazolin-4-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/657269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(7-Fluoro-quinazolin-4-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 59551736—
SolventSodium BicarbonateHCID 516892—
Product4-[7-(2-Hydroxy-ethoxy)-quinazolin-4-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 5955176881%

Reaction Steps

KOtBu (1.17 g, 10.4 mmol) was added to ethylene glycol (10 mL, 179 mmol) to provide a homogeneous solution. 4-(7-fluoro-quinazolin-4-yl)-piperidine-1-carboxylic acid tert-butyl ester (2.61 g, 7.89 mmol), as prepared in Example 65b, was added, and the opaque white slurry was stirred at rt for 3.5 hr. DMSO (5 mL) was then added, and the mixture stirred at 110° C. for 20 min at which point it became a homogeneous solution. The reaction was then stirred at rt overnight, at which point it became a translucent white slurry. The mixture was then diluted with 0.1M NaHCO3 and extracted with EtOAc (2×50 mL). The combined organic layers were washed with 0.1M NaHCO3 (1×100 mL), dried (Na2SO4), concentrated, and dissolved in ˜15 mL toluene. The title compound crystallized upon standing at rt, was filtered, and the crystalline filter cake washed with toluene (1×10 mL). The filter cake was dried under high vacuum at 100° C. to afford the title compound as a white powder (2.38 g, 81%). LC/MS (ESI): calc mass 373.2, found 374.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071768B2
Source datasetuspto-grants-2011_12
ORD IDord-72a0875d9276427d894c49bdf23130f0
Source noteuspto-grants-2011_12