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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485631Generated: November 1, 2026

N-[(4-Bromophenyl)(dimethylamino)oxo-lambda6-sulfanylidene]-2,2,2-trifluoroacetamide → N-({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)phenyl]phenyl}(dimethylamino)oxo-lambda6-sulfanylidene)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/1485631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[(4-Bromophenyl)(dimethylamino)oxo-lambda6-sulfanylidene]-2,2,2-trifluoroacetamideHCID 118863932—
Reactant(3R,3aR,6R,6aR)-6-(6-Chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-olHCID 123678375—
Solvent1,4-DioxaneHCID 31275—
ProductN-({4-[4-(2-{[(3R,3aR,6R,6aR)-6-Hydroxy-hexahydrofuro[3,2-b]furan-3-yl]oxy}-6-chloro-3-{[2-(trimethylsilyl)ethoxy]methyl}imidazo[4,5-b]pyridin-5-yl)phenyl]phenyl}(dimethylamino)oxo-lambda6-sulfanylidene)-2,2,2-trifluoroacetamideHCID 131736745—

Reaction Steps

The title compound is prepared from (3R,3aR,6R,6aR)-6-(6-chloro-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and N-[(4-bromophenyl)-(dimethylamino)oxo-λ6-sulfanylidene]-2,2,2-trifluoroacetamide following a procedure analogous to that described for Intermediate 3 (Step 3) using 1,4-dioxane as a solvent. LC (method 1): tR=1.22 min; Mass spectrum (ESI+): m/z=782 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422312B2
Source datasetuspto-grants-2016_08
ORD IDord-8d5b489075ff4310879d873f4f403540
Source noteuspto-grants-2016_08