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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715578Generated: November 2, 2026

2-((3R,3aR,6R,6aS)-6-(tert-butyldimethylsilyloxy)hexahydrofuro[3,2-b]furan-3-yloxy)-6-chloro-5-iodo-3-((2-(tri-methylsilyl)ethoxy)methyl)-3H-imidazo[4,5-b]pyridine → HCID 178455385, compound

https://huagongshe.com/reaction/715578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((3R,3aR,6R,6aS)-6-(tert-butyldimethylsilyloxy)hexahydrofuro[3,2-b]furan-3-yloxy)-6-chloro-5-iodo-3-((2-(tri-methylsilyl)ethoxy)methyl)-3H-imidazo[4,5-b]pyridineHCID 123454612—
ReactantHCID 178431055HCID 178431055—
ProductHCID 178455385HCID 178455385—

Reaction Steps

The title compound is prepared from 2-((3R,3aR,6R,6aS)-6-(tert-butyldimethylsilyloxy)hexahydrofuro[3,2-b]furan-3-yloxy)-6-chloro-5-iodo-3-((2-(tri-methylsilyl)ethoxy)methyl)-3H-imidazo[4,5-b]pyridine and (cis)-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclohexanol following a procedure analogous to that described for Intermediate 7 Step 2. LC (method 5): tR=1.21 min; Mass spectrum (ESI+): m/z=716 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187477B2
Source datasetuspto-grants-2015_11
ORD IDord-f7f120fbf9374ecea7ac384302c52bd4
Source noteuspto-grants-2015_11