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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056985Generated: October 31, 2026

6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-one → 4-[4-(Cyclopropylmethoxy)-1-methyl-1H-indazol-5-yl]-6-methyl-1-[(4-methylphenyl)sulfonyl]-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one

https://huagongshe.com/reaction/1056985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-oneHCID 86721062—
Reactant5-Bromo-4-(cyclopropylmethoxy)-1-methyl-1H-indazoleHCID 118093942—
Product4-[4-(Cyclopropylmethoxy)-1-methyl-1H-indazol-5-yl]-6-methyl-1-[(4-methylphenyl)sulfonyl]-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-oneHCID 118093818—

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-1-[(4-methylphenyl)sulfonyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one as the starting materials. LCMS calculated for C27H27N4O4S (M+H)+: m/z=503.2. found: 503.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399640B2
Source datasetuspto-grants-2016_07
ORD IDord-ac7103c3cde0430f93aed75ad424327a
Source noteuspto-grants-2016_07