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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646686Generated: October 30, 2026

Dichloromethane → Phenylmethyl 4-{5-amino-6-[(methylamino)carbonyl]pyrazin-2-yl}benzoate

https://huagongshe.com/reaction/646686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant4-(Benzyloxycarbonyl)phenylboronic AcidHCID 2773251—
Reactant3-Amino-6-bromo-N-methylpyrazine-2-carboxamideHCID 15148121—
SolventDimethylformamideHCID 6228—
ProductPhenylmethyl 4-{5-amino-6-[(methylamino)carbonyl]pyrazin-2-yl}benzoateHCID 6865028359.7%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred mixture of 3-amino-6-bromo-N-methyl-2-pyrazinecarboxamide (0.577 g, 2.5 mmol), 4-benzyloxycarbonylphenylboronic acid (0.768 g, 3.0 mmol), triethylamine (1.01 g, 10 mmol) in 10 mL of DMF was added [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with dichloromethane (1:1), (20.4 mg, 0.025 mmol). The stirred mixture was warmed to 80-90° C. for 12 h and then concentrated on a rotary evaporator under reduced pressure. The residue was dissolved in 50 mL of EtOAc, washed with brine (30 mL). The organic layer was filtered through celite, and then dried over anhydrous sodium sulfate. Filtration, concentration and column chromatography on silica EtOAc) gave a solid (450 mg, 59.7% yield). 1H NMR (400 MHz; DMSO-d6): 8.91 (s, 1H); 8.84 (br s, 1H); 8.33 (d, 2H); 8.02 (d, 2H); 7.30-7.48 (m, 5H); 5.38 (s, 2H); 2.86 (s, 3M); MS (EI) for C20H15N4O3: 363 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-d326b60a4af646aa98e463b402cc2bcb
Source noteuspto-grants-2010_04