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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056997Generated: October 31, 2026

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

https://huagongshe.com/reaction/1056997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-fluoro-N-methyl-2-nitroanilineHCID 118093832—
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-[2-Fluoro-4-(methylamino)-3-nitrophenyl]-6-methyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-oneHCID 123586401—

Reaction Steps

This compound was synthesized according to the procedure of Example 10, Step 5, using 4-bromo-3-fluoro-N-methyl-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 C21H28FN4O4Si (M+H)+: m/z=447.2. found: 447.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399640B2
Source datasetuspto-grants-2016_07
ORD IDord-6cfa683b8471443b9695c343f6c84ba3
Source noteuspto-grants-2016_07