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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930593Generated: October 28, 2026

HCID 57840589, compound → HCID 136174641, compound

https://huagongshe.com/reaction/930593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57840589HCID 57840589—
Reactant2-(3-(1H-imidazol-2-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl)acetic acidHCID 136174646—
ProductHCID 136174641HCID 136174641—

Reaction Steps

The title compound was prepared following Protocol A. (R)-1-(4-Chloro-3-methoxyphenyl)-2-methylpiperazine and [3-(1H-imidazol-2-yl)pyrazolo[3,4-b]pyridin-1-yl]acetic acid were used as the coupling components. The crude product was purified by silica gel chromatography (1% to 7.5% MeOH in CH2Cl2) to provide 1-[(R)-4-(4-chloro-3-methoxyphenyl)-3-methylpiperazin-1-yl]-2-[3-(1H-imidazol-2-yl)-pyrazolo[3,4-b]pyridin-1-yl]ethanone as a tan solid: 1H NMR (CDCl3, 400 MHz) δ□ 8.76 (d, 0.6H), 8.66 (dd, 0.3H), 8.57-8.54 (m, 1H), 7.29-7.19 (m, 4H), 6.48-6.40 (m, 2H), 5.53-5.40 (m, 2H), 4.26 (br. d, 0.6H), 4.00 (br. d, 0.6H), 3.88 (s, 1.3H), 3.86 (s, 1.7H), 3.80-3.49 (m, 3.2H), 3.33 (br. s, 0.6H), 3.17-3.14 (m, 2H), 1.51-1.42 (m, 3H); LC/MS m/z (M+H)+ 466.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296740B2
Source datasetuspto-grants-2016_03
ORD IDord-be32495e33974ef6bcce3b20b582fd2f
Source noteuspto-grants-2016_03