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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204408Generated: October 31, 2026

(2,4-Dimethoxypyrimidin-5-yl)boronic acid → HCID 86703220, compound

https://huagongshe.com/reaction/2204408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,4-Dimethoxypyrimidin-5-yl)boronic acidHCID 2736209—
Reactant4-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amineHCID 59198404—
Reactant2-bromo-5-(5-chloro-2-methyl-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-oneHCID 86703169—
ReactantHCID 86703221HCID 86703221—
ProductHCID 86703220HCID 86703220—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Example 25 but 2-bromo-6-(4-chloro-3-fluoro-phenyl)-5-(5-chloro-1-methyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one (Intermediate BA) and 2,4-dimethoxypyrimidine-5-boronic acid were used instead of 2-bromo-5-(5-chloro-2-methyl-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one and 4-methoxy-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrimidin-2-ylamine respectively. The title compound was obtained as a white solid. tR: 1.15 min (HPLC 3); ESI-MS: tR=1.13 min, [M+H]+ 572/574/576 (LC-MS 1); TLC: Rf=0.25 (EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-6ae19c5da80b47be98f376df2035c4c4
Source noteuspto-grants-2016_06