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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261237Generated: October 27, 2026

2-Bromothiazole → 7-Chloro-2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)thieno[3,2-b]pyridine

https://huagongshe.com/reaction/1261237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiazoleHCID 76430—
Reactant7-Chloro-2-(1,3-thiazol-2-yl)thieno[3,2-b]pyridineHCID 22143663—
Reactant7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridineHCID 57516658—
Reactant2-Bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazoleHCID 59424542—
Product7-Chloro-2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)thieno[3,2-b]pyridineHCID 59424670—

Reaction Steps

Starting from the compound 98 (scheme 19) and following the procedure described above for the synthesis of compound 10 (example 12, scheme 2) but substituting 2-bromothiazole in the step 2 for the bromide 108, title compound 109 was obtained as a white solid (22 mg, 41% yield). MS (m/z) 366.1/368.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470850B2
Source datasetuspto-grants-2013_06
ORD IDord-74da1a2a3f844ef4b77670cb65bbae2f
Source noteuspto-grants-2013_06