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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499565Generated: October 31, 2026

Diisopropylethylamine → HCID 86726788, compound

https://huagongshe.com/reaction/1499565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 227251—
Reactant2,6-Difluorophenylboronic acidHCID 2734336—
CatalystBis(tri-tert-butylphosphine)palladium(0)HCID 2734558—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86726788HCID 8672678891%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of (2,6-difluorophenyl)boronic acid (270 mg, 1.7 mmol), methyl 3-amino-6-bromopyrazine-2-carboxylate (from Ark Pharm, 250 mg, 1.1 mmol), bis(tri-tert-butylphosphine) palladium (82 mg, 0.16 mmol), and DIPEA (370 μL, 2.1 mmol) in 1,4-dioxane (4 mL) and water (320 μL) in a vial was deoxygenated and purged with nitrogen several times. The vial was sealed and the reaction mixture was heated at 100° C. in the sealed vial for 14 h. The crude reaction mixture was filtered through a pad of diatomaceous earth and the inorganics were washed thoroughly with EtOAc. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography (40 g silica gel column, eluting with 0-50% EtOAc in hexanes) to afford the sub-title compound (258 mg, 91% yield). LC/MS (ESI) calc. for C12H10F2N3O2(M+H)+: m/z=266.1. found: 266.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-927f8bafdb854887924b2a9886e1f724
Source noteuspto-grants-2015_12