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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204385Generated: October 30, 2026

2-Bromo-3-methoxypyridine → HCID 72205350, compound

https://huagongshe.com/reaction/2204385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-methoxypyridineHCID 90364—
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 86703194HCID 86703194—
ProductHCID 72205350HCID 72205350—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Example 17 but 2-bromo-3-methoxy-pyridine [24100-18-3] and 5-(5-chloro-2-methyl-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one (Step 113.1) 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: 6.54 min (HPLC 2); ESI-MS: tR=1.27 min, [M+H]+ 506/508/510 (LC-MS 1); TLC: Rf=0.21 (98:2 CH2Cl2/MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-6bb1626a076c4aaca55113c1a48d9b40
Source noteuspto-grants-2016_06