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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347280Generated: October 30, 2026

Potassium Carbonate → HCID 11234522, compound

https://huagongshe.com/reaction/347280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantChloropyrazineHCID 73277—
ReactantHCID 86596746HCID 86596746—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
ProductHCID 11234522HCID 1123452232%

Reaction Conditions

Temperature240 °C

Reaction Steps

(S)-2-Amino-4,4-dimethyl-pentanoic acid [2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethyl]-amide (20 mg, 0.066 mmol) was dissolved in DMF (0.7 mL) containing equimolar amounts of 2-chloropyrazine (6 μL, 0.066 mmol), 0.1 equivalents of CuI (1.3 mg, 0.006 mmol), and 1.5 equivalents of potassium carbonate (13.9 mg, 0.099 mmol). The mixture was stirred and heated by microwave to 240° C. for 30 minutes. After completion the mixture was purified by reverse phase LC to afford (S)-4,4-Dimethyl-2-(pyrazin-2-ylamino)-pentanoic acid [2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethyl]-amide 2 (8.3 mg, 0.02 mmol, 32%): 1H-NMR (400 MHz, CD3OD) δ=8.37 (m, 2H), 6.82–6.41 (m, 4H), 4.57 (dd, J=9.2, J=3.2, 1H), 3.42 (t, J=6.2, 2H), 3.36 (t, J=8.2, 2H), 3.14 (m, 2H), 2.88 (t, J=8.2, 2H), 1.83–1.62 (m, 2H), 0.96 (s, 9H). MS calcd. for C21H29FN5O (M+H+) 386.23. found 386.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173051B2
Source datasetuspto-grants-2007_02
ORD IDord-5f83ea28729544dbbb67708aa0dc204a
Source noteuspto-grants-2007_02