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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056956Generated: November 1, 2026

4-Bromo-3-(2,4-difluorophenoxy)-2-nitroaniline → 4-[4-Amino-2-(2,4-difluorophenoxy)-3-nitrophenyl]-6-methyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one

https://huagongshe.com/reaction/1056956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-(2,4-difluorophenoxy)-2-nitroanilineHCID 118093920—
Reactant6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-oneHCID 123210853—
Product4-[4-Amino-2-(2,4-difluorophenoxy)-3-nitrophenyl]-6-methyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-oneHCID 123242082—

Reaction Steps

This compound was synthesized according to the procedure of Example 10, Step 5, using 4-bromo-3-(2,4-difluorophenoxy)-2-nitroaniline and 6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one as the starting materials. LCMS calculated for C26H29F2N4O5Si (M+H)+: m/z=543.2. found: 543.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399640B2
Source datasetuspto-grants-2016_07
ORD IDord-017cfd004877476d8c38f8803db4752c
Source noteuspto-grants-2016_07