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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523739Generated: October 30, 2026

Dichloromethane → HCID 90313799, compound

https://huagongshe.com/reaction/1523739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Chloro-2-fluorophenyl)boronic acidHCID 4193595—
Reactant6-Amino-3-bromo-2-pyrazinecarbonitrileHCID 87171680—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
ProductHCID 90313799HCID 90313799—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 200 mL round-bottomed flask were added a stirbar, 5-amino-3-cyano-2-bromopyrazine (4.09 g, 20.5 mmol), 4-chloro-2-fluorophenylboronic acid (3.90 g, 22.4 mmol), Pd(dppf)Cl2.CH2Cl2 (839 mg, 1.03 mmol) and K2CO3 (8.36 g, 60.5 mmol). The flask was flushed with nitrogen and then charged with toluene (17.5 mL), water (17.5 mL) and DMF (10.5 mL), all of which were sparged with N2. The flask was heated at 80° Celsius for 19 hours before cooling to rt and adding MgSO4 until the mixture was a thick paste. The reaction mixture was then stirred with EtOAc and filtered through a thick pad of celite. The pad was rinsed with EtOAc until the filtrate was colorless. The filtrate was concentrated to dryness and subjected to FCC to give 6-amino-3-(4-chloro-2-fluorophenyl)pyrazine-2-carbonitrile. MS (ESI): mass calcd. for C11H6ClFN4, 248.03; m/z found, 249.0 [M+H]+. 1H NMR (500 MHz, DMSO-d6) δ 8.22 (s, 1H), 7.67-7.60 (m, 2H), 7.46 (dd, J=8.4, 2.0, 1H), 7.37 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-cba445e151dc482eb55db1ae506f4cb7
Source noteuspto-grants-2015_07