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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204395Generated: November 3, 2026

2-Methoxyphenylboronic acid → HCID 86703205, compound

https://huagongshe.com/reaction/2204395

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxyphenylboronic acidHCID 2733958—
Reactant(5-Cyano-2-Methoxyphenyl)Boronic AcidHCID 23005336—
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 86703206HCID 86703206—
ProductHCID 86703205HCID 86703205—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Example 17 but 2-bromo-5-(5-chloro-1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-6-(4-chloro-2-methyl-phenyl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one (Intermediate N) and 2-methoxyphenylboronic 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 5-cyano-2-methoxyphenylboronic acid respectively. The title compound was obtained as a light yellow solid. tR: 7.25 min (HPLC 2); ESI-MS: tR=1.21 min, [M+H]+ 536/538 (LC-MS 1); TLC: Rf=0.20 (EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-35a51d3ec05f4631b89ac4de9549a268
Source noteuspto-grants-2016_06