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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38329Generated: October 29, 2026

4-Chloro-5-iodo-2-(methylthio)pyrimidine → (4-Chloro-2-methylsulfanyl-pyrimidin-5-yl)-(2-isopropyl-4,5-dimethoxy-phenyl)-methanol

https://huagongshe.com/reaction/38329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-5-iodo-2-(methylthio)pyrimidineHCID 13636519—
Reactant2-Isopropyl-4,5-dimethoxy-benzaldehydeHCID 54145114—
ReactantHCID 178418365HCID 178418365—
SolventTetrahydrofuranHCID 8028—
Product(4-Chloro-2-methylsulfanyl-pyrimidin-5-yl)-(2-isopropyl-4,5-dimethoxy-phenyl)-methanolHCID 5959861782%

Reaction Steps

To a solution of 4-chloro-5-iodo-2-methylsulfanyl-pyrimidine (1.10 g, 3.9 mmol) in 20 mL THF at −40° C. was added isopropyl magnesium bromide (2.3 mL, 2 M in THF)) over 5 minutes. After 30 minutes, 2-isopropyl-4,5-dimethoxy-benzaldehyde from step 3 (1.04 g, 4.6 mmol) was added and the solution was warmed to room temperature. The mixture was quenched by the addition of brine, and extracted with CH2Cl2. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. Purification via flash chromatography (ethyl acetate) afforded (4-chloro-2-methylsulfanyl-pyrimidin-5-yl)-(2-isopropyl-4,5-dimethoxy-phenyl)-methanol (1.168 g, 82%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524725B2
Source datasetuspto-grants-2013_09
ORD IDord-50d76addffd549c580e4714bf8ebf9d3
Source noteuspto-grants-2013_09