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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204407Generated: November 1, 2026

(2,4-Dimethoxypyrimidin-5-yl)boronic acid → 5-(2,4-dimethoxy-pyrimidin-5-yl)-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/2204407

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,4-Dimethoxypyrimidin-5-yl)boronic acidHCID 2736209—
Reactant(5-Cyano-2-Methoxyphenyl)Boronic AcidHCID 23005336—
ReactantMethyl 5-bromo-1-isopropyl-1H-pyrrole-3-carboxylateHCID 86703102—
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—
Product5-(2,4-dimethoxy-pyrimidin-5-yl)-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl esterHCID 86703219—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Example 17 but 5-bromo-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl ester (Step D4) 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 5-cyano-2-methoxyphenylboronic acid respectively. The title compound was obtained as a yellow solid. tR: 0.97 min (HPLC 3); ESI-MS: tR=0.97 min, [M+H]+ 306 (LC-MS 1); TLC: Rf=0.43 (1:1 EtOAc/heptanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-6bffd7ad9dff4276bc7a41bccb9b80d7
Source noteuspto-grants-2016_06