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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972713Generated: October 30, 2026

Potassium Iodide → HCID 58529656, compound

https://huagongshe.com/reaction/1972713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-{4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl}-2-chloroethan-1-oneHCID 58529311—
ReactantHCID 58529880HCID 58529880—
SolventDimethylformamideHCID 6228—
ProductHCID 58529656HCID 5852965681%

Reaction Steps

To a solution of 1-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-2-chloroethanone (1.00 g, 4.75 mmol), K2CO3 (1.97 g, 14.2 mmol) and potassium iodide (79 mg, 0.47 mmol) in DMF (20 mL), was added 1-benzyl-3-({[tert-butyl(dimethyl)silyl]oxy}methyl)piperazine (1.53 g, 4.79 mmol, prepared by the method of Naylor et al J. Med. Chem. 36, 2075). The reaction was allowed to stir for 17 hours. The mixture was partitioned between ethyl acetate (200 mL) and saturated, aqueous Na2CO3 solution (100 mL). The layers were separated and the organic was washed with brine, dried (Na2SO4), and evaporated. The crude material was purified by ISCO® chromatography using a gradient elution from 50% to 100% ethyl acetate in hexanes to obtain 1.9 g (81%) of the desired product LC-MS [M+H]+=495.6, RT=2.56 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-3b4125b3c1ed4951ab17abb723b4d053
Source noteuspto-grants-2013_04