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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204382Generated: October 31, 2026

(5-Cyano-2-Methoxyphenyl)Boronic Acid → HCID 86703188, compound

https://huagongshe.com/reaction/2204382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Cyano-2-Methoxyphenyl)Boronic AcidHCID 23005336—
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 86703189HCID 86703189—
ProductHCID 86703188HCID 86703188—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Example 17 but 2-bromo-6-(4-chloro-phenyl)-1-isopropyl-5-(1-methyl-6-oxo-piperidin-3-yl)-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one (Intermediate Q) and 4-methoxy-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrimidin-2-ylamine (Intermediate U) 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 5-cyano-2-methoxyphenylboronic acid respectively. The title compound was obtained as a beige solid. tR: 2.35 min (HPLC 5); ESI-MS: tR=0.81 min, [M+H]+ 509/511 (LC-MS 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-0d9fb42aef9a48a3bef3ddc83bfde922
Source noteuspto-grants-2016_06