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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970950Generated: October 30, 2026

Trimethylsilyl iodide → HCID 178424664, compound

https://huagongshe.com/reaction/1970950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 44197797HCID 44197797—
SolventDichloromethaneHCID 6344—
ProductHCID 178424664HCID 178424664—

Reaction Steps

A solution of (4-{5-[6-benzyloxy-2-(6-methyl-pyridin-2-yl)-pyrimidin-4-yl]-pyridin-3-yl}-phenyl)-(4-isopropyl-piperazin-1-yl)-methanone (Example 8) (1 eq, 30 mg) in dry DCM (0.6 ml) under an atmosphere of N2 is treated with trimethylsilyl iodide (12 eq, 83.6 μl). After stirring at RT overnight, the reaction is quenched by addition of MeOH (5 ml) and stirring continued for 45 minutes. The solvent is removed in vacuo and the residue is loaded onto a SCX-2 cartridge (1 g) eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are combined and concentrated in vacuo and dried under vacuum overnight to afford the title compound [M+H]+=495 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431578B2
Source datasetuspto-grants-2013_04
ORD IDord-309abb9c73fe40bb9f8b18fe318c2a53
Source noteuspto-grants-2013_04