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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81832Generated: October 27, 2026

Sodium Bicarbonate → 5-(5-Furan-2-yl-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/81832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantFuran-2-boronic acidHCID 2734357—
Reactant5-(5-Iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamineHCID 15953802—
Solvent1,4-DioxaneHCID 31275—
Product5-(5-Furan-2-yl-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamineHCID 5732911315.6%

Reaction Conditions

Temperature105 °C

Reaction Steps

5-(5-Iodo-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine (400 mg, 1 mmol), furan 2-boronic acid (285 mg, 1.5 mmol) and Pd(Ph3)2Cl2 (50 mg) were taken up in 13 mL of degassed dioxane in a screw cap pressure flask. Sodium bicarbonate (2 mL of 2M aqueous solution) was added, and the reaction mixture was heated to 105° C. for 40 hours. The reaction mixture was cooled and partitioned between water and ethyl acetate. The organic phase was separated, dried (MgSO4), filtered, and evaporated under reduced pressure. The residue was purified by flash chromatography (3% to 5% MeOH in methylene chloride with 1% ammonium hydroxide) to yield 53 mg of 5-(5-Furan-2-yl-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine (M+H)=339. Mp=253.7-254.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846705B2
Source datasetuspto-grants-2014_09
ORD IDord-007f90170ae04ccd8bb7f3b0dcbe238c
Source noteuspto-grants-2014_09