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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494000Generated: October 31, 2026

(2-Bromoethoxy)-tert-butyldimethylsilane → [6-Bromo-1-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-methanone

https://huagongshe.com/reaction/494000

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
Reactant[6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-Dioxo-1lambda6-thiomorpholin-4-yl)-methanoneHCID 16739609—
Product[6-Bromo-1-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-methanoneHCID 67073382—

Reaction Steps

In analogy to the procedure described for the synthesis of example 1, step 1, the title compound was synthesized from [6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-dioxo-1λ6-thiomorpholin-4-yl)-methanone (Example 6, step 4) and (2-bromoethoxy)-tert-butyldimethylsilane. The desired product was obtained in a yield of 50% as colorless oil. MS (m/e): 656.4 (M+H, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538101B2
Source datasetuspto-grants-2009_05
ORD IDord-2eda7f77f6a248a597c42f080126c08f
Source noteuspto-grants-2009_05