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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056986Generated: October 31, 2026

5-Bromo-4-(cyclopropylmethoxy)-1-methyl-1H-indazole → 4-(4-(cyclopropylmethoxy)-1-methyl-1H-indazol-5-yl)-6-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[3,4-c]pyridin-7(6H)-one

https://huagongshe.com/reaction/1056986

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-4-(cyclopropylmethoxy)-1-methyl-1H-indazoleHCID 118093942—
Reactant6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrazolo[3,4-c]pyridin-7-oneHCID 123366289—
Product4-(4-(cyclopropylmethoxy)-1-methyl-1H-indazol-5-yl)-6-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[3,4-c]pyridin-7(6H)-oneHCID 123838973—

Reaction Steps

This compound was synthesized according to the procedure of Example 10, Step 5, using 5-bromo-4-(cyclopropylmethoxy)-1-methyl-1H-indazole and 6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrazolo[3,4-c]pyridin-7-one as the starting materials. LCMS calculated for C25H34N5O3Si (M+H)+: m/z=480.2. found: 480.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399640B2
Source datasetuspto-grants-2016_07
ORD IDord-349255b89313438fbc34461dcbdc3302
Source noteuspto-grants-2016_07