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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434932Generated: November 2, 2026

4-Chloro-2-methylthiopyrimidine → HCID 57936139, compound

https://huagongshe.com/reaction/1434932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-methylthiopyrimidineHCID 97113—
Reactant1-(Triisopropylsilyl)pyrrole-3-boronic acidHCID 2763303—
ProductHCID 57936139HCID 5793613995%

Reaction Steps

The title compound was prepared analogous to Step A of Method B, starting from [1-[tris(1-methylethyl)silyl]-1H-pyrrol-3-yl]-boronic acid and 4-chloro-2-methylsulfanyl-pyrimidine. Under the reaction conditions, the triisopropylsilyl protecting group was cleaved. Yield: 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615562B2
Source datasetuspto-grants-2009_11
ORD IDord-50ae74be66bf46e9a45473fcec975560
Source noteuspto-grants-2009_11