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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677474Generated: October 30, 2026

1-Methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine → (1-Methyl-cyclohexyl)-{2-[4-(4-methyl-piperazin-1-yl)-phenyl]-5H-pyrrolo[2,3-b]pyrazin-7-yl}-methanone

https://huagongshe.com/reaction/1677474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazineHCID 17998905—
Reactant(2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)-(1-methyl-cyclohexyl)-methanoneHCID 44199730—
Product(1-Methyl-cyclohexyl)-{2-[4-(4-methyl-piperazin-1-yl)-phenyl]-5H-pyrrolo[2,3-b]pyrazin-7-yl}-methanoneHCID 59540597—

Reaction Steps

(1-Methyl-cyclohexyl)-{2-[4-(4-methyl-piperazin-1-yl)-phenyl]-5H-pyrrolo[2,3-b]pyrazin-7-yl}-methanone was prepared starting from (2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)-(1-methyl-cyclohexyl)-methanone and 1-methyl-4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-piperazine following general procedures as described in these Examples. MP 225-226° C., M+H=418.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008298B2
Source datasetuspto-grants-2011_08
ORD IDord-cd0bf5ff63d840c18633412fa72ba866
Source noteuspto-grants-2011_08