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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235073Generated: October 30, 2026

Toluene → HCID 23353221, compound

https://huagongshe.com/reaction/235073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 23353262HCID 23353262—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23353221HCID 2335322135.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Ethyl 3-aminothieno[2,3-b]pyrazine-2-carboxylate (0.500 g, 2.24 mmol) was dissolved in 15 ml THF under nitrogen. The solution was cooled to -78° C and dropwise treated with 4.9 ml 0.5M KHMDS in toluene (2.46 mmol). The resulting purple reaction mixture was allowed to warm to rt, treated with 2-iodopropane (0.46 s g, 2.69 mmol) and then brought to reflux for 48h. After the addition of 1 ml EtOH, the reaction mixture was concentrated and applied directly to a silica gel column. Elution with a solvent gradient from 10:1 to 4:1 hexanes: ethyl acetate gave the title compound (0.210 g, 35%). 1H NMR (300 MHz, CDCl3) δ1.30 (d, 6H), 1.40 (t, 3H), 4.37 (q, 2H), 5.27 (dh, 1H), 7.42 (br d, 1H), 8.55 (d, 1H), 8.58 (d, 1H). MS (DCI/NH3) m/e 266 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597823
Source datasetuspto-grants-1997_01
ORD IDord-1c87af0b72fa49e3875185d10a10a988
Source noteuspto-grants-1997_01