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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389477Generated: October 30, 2026

Potassium Iodide → tert-Butyl {2-[3-(2,3-dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetate

https://huagongshe.com/reaction/2389477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Chloro-propyl)-3-oxo-2,3-dihydro-indazole-1-carboxylic acid ethyl esterHCID 69314746—
ReactantHCID 178451223HCID 178451223—
SolventAcetoneHCID 180—
Producttert-Butyl {2-[3-(2,3-dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetateHCID 86620027—

Reaction Steps

A mixture of tert-butyl (2-mercapto-benzoimidazol-1-yl)-acetate (Intermediate 3-I, 66 mg, 0.25 mmol), 2-(3-chloro-propyl)-3-oxo-2,3-dihydro-indazole-1-carboxylic acid ethyl ester (alkylating agent G-01d, 70 mg, 0.25 mmol), a few crystals of potassium iodide and K2CO3 (69 mg, 0.5 mmol) in acetone (1 ml) is refluxed overnight. Evaporation of the solvent under a stream of air affords a residue that is purified by flash-chromatography on silica-gel (AcOEt/heptane, 3:2), yielding the title compound as a colourless oil: tR=2.75 min (LC-2), ESI-MS (pos.): m/z 511.15 [M+H]+; 1H-NMR (CDCl3): δ (ppm) 1.37 (s, 9H, tBu), 1.37 (t, 3H, CH3), 2.14 (quint., 2H, CH2CH2N), 3.28 (m, 2H, SCH2), 4.30-4.40 (m, 4H), 4.69 (s, 2H, CH2CO2), 7.10 (m, 3Harom), 7.26 (t, 1Harom), 7.55 (m, 2Harom), 7.81 (t, 2Harom).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273740B2
Source datasetuspto-grants-2012_09
ORD IDord-8c7af3d463dc427fae97448ada1b2238
Source noteuspto-grants-2012_09