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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036155Generated: October 31, 2026

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine → 5-(7-chloro-2,2-difluoro-3H-benzo[3,4-e]1,4-dioxin-6-yl)pyrazine-2-ylamine

https://huagongshe.com/reaction/1036155

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amineHCID 17998987—
Reactant6-bromo-7-chloro-2,2-difluoro-3H-benzo[e]1,4-dioxinHCID 58487468—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product5-(7-chloro-2,2-difluoro-3H-benzo[3,4-e]1,4-dioxin-6-yl)pyrazine-2-ylamineHCID 584867179%

Reaction Conditions

Temperature85 °C

Reaction Steps

5-Aminopyrazine-2-boronic acid pinacol ester (62 mg, 0.28 mmol) and 254 (67 mg, 0.23 mmol) were dissolved in 2 mL 1,4-dioxane and 2 mL MeCN. Next 1 ml of 2 M K3PO3 was added and the mixture was then bubbled with Ar for 2 min before bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (A-Phos, 70 mg, 0.1 mmol) was added. The reaction was then heated at 85° C. for 2 h. The reaction mixture was cooled and then worked-up with EtOAc extraction. The product was purified by flash column and afforded 256 (6 mg, 9%) as a yellow wax.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546403B2
Source datasetuspto-grants-2013_10
ORD IDord-d287beac00ad4292be759cd464a4dc2d
Source noteuspto-grants-2013_10