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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643511Generated: October 30, 2026

Ethyl Acetate → {4-[3-(2-Cyano-pyrimidin-4-yloxy)-phenoxymethyl]-benzyl}carbamic acid tert-butyl ester

https://huagongshe.com/reaction/643511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CyanideHCID 9032—
ReactantDabcoHCID 9237—
Reactant{4-[3-(2-Chloro-pyrimidin-4-yloxy)-phenoxymethyl]-benzyl}carbamic acid tert-butyl esterHCID 86622897—
Solvent(Methanesulfinyl)methane--water (1/1)HCID 23503278—
Product{4-[3-(2-Cyano-pyrimidin-4-yloxy)-phenoxymethyl]-benzyl}carbamic acid tert-butyl esterHCID 68579046—

Reaction Steps

{4-[3-(2-Chloro-pyrimidin-4-yloxy)-phenoxymethyl]-benzyl}carbamic acid tert-butyl ester (126 mg; 0.285 mmol; Stage 5.2), DABCO (16 mg; 0.143 mmol) and KCN (38 mg; 0.584 mmol) are dissolved in DMSO/water 4:1 (4 mL) at rt under an atmosphere of argon. After 20 min, more DABCO (16 mg) is added and the reaction is continued for a total of 1 h 50 min. The reaction mixture is poured onto brine, taken up into EtOAc, washed with water and brine and dried (Na2SO4). After filtration, the solvent is removed under reduced pressure and the crude product is purified by flash chromatography over silica gel (eluting with Hexane/EtOAc 80:20) to give the title compound of Stage 5.3 as an oil; ES-MS: [M−H]−; m/z=431; Rf (Hexane/EtOAc 1:1)=0.45; HPLC: AtRet=5.19 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700605B2
Source datasetuspto-grants-2010_04
ORD IDord-e3c8029a486b4cc7a4b8b09abcfbcc89
Source noteuspto-grants-2010_04