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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204376Generated: October 31, 2026

2-Methoxyphenylboronic acid → HCID 86703178, compound

https://huagongshe.com/reaction/2204376

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 86703179HCID 86703179—
ProductHCID 86703178HCID 86703178—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Example 17 but 2-[2-bromo-6-(4-chloro-phenyl)-1-isopropyl-4-oxo-4,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-5-yl]-4-chloro-benzonitrile (Intermediate AB) 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 brown solid. tR: 7.83 min (HPLC 2); ESI-MS: tR=1.32 min, [M+H]+ 516/518 (LC-MS 1); TLC: Rf=0.26 (1:4 EtOAc/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-ad981105e30240b2b9c3321e00868abe
Source noteuspto-grants-2016_06