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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677246Generated: October 31, 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/1677246

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 numberUS08008313B2
Source datasetuspto-grants-2011_08
ORD IDord-c4f2bd8fac3a4ae5bf6815f0e58cf862
Source noteuspto-grants-2011_08