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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485610Generated: November 2, 2026

N'-(4-Bromophenyl)-N-methyl-methanesulfonimidamide → 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}-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]phenyl}-N-methyl-methanesulfonimidamide

https://huagongshe.com/reaction/1485610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-(4-Bromophenyl)-N-methyl-methanesulfonimidamideHCID 118863941—
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—
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}-3H-imidazo[4,5-b]pyridin-5-yl)phenyl]phenyl}-N-methyl-methanesulfonimidamideHCID 131736736—

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)-N-methyl-methanesulfonimidamide following a procedure analogous to that described for Intermediate 3 (Step 3). LC (method 1): tR=1.07 min; Mass spectrum (ESI+): m/z=686 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422312B2
Source datasetuspto-grants-2016_08
ORD IDord-9346e2c6fc074ffcb2266d627ca5dc9b
Source noteuspto-grants-2016_08