Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416509Generated: October 25, 2026

(2-Bromoethoxy)-tert-butyldimethylsilane → 5-Chloro-thiophene-2-carboxylic acid {2-[[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(1-isopropyl-piperidin-4-yl)-sulfamoyl]-ethyl}-amide

https://huagongshe.com/reaction/416509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
Reactant5-Chloro-Thiophene-2-Carboxylic Acid [2-(1--Isopropyl-Piperidin-4-Ylsulfamoyl)-Ethyl]-AmideHCID 11990478—
Product5-Chloro-thiophene-2-carboxylic acid {2-[[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(1-isopropyl-piperidin-4-yl)-sulfamoyl]-ethyl}-amideHCID 66624617—

Reaction Steps

5-Chloro-thiophene-2-carboxylic acid {2-[[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(1-isopropyl-piperidin-4-yl)-sulfamoyl]-ethyl}-amide was prepared by an analogous procedure as described in example 15 starting from 2.3 ml (3.5 equiv.) (2-bromo-ethoxy)-tert-butyl-dimethyl-silane and 1.2 g (3.05 mmol) 5-chloro-thiophene-2-carboxylic acid [2-(1-isopropyl-piperidin-4-ylsulfamoyl)-ethyl]-amide. 5-Chloro-thiophene-2-carboxylic acid {2-[[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(1-isopropyl-piperidin-4-yl)-sulfamoyl]-ethyl}-amide was obtained as crude material which was pure enough for further transformations.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088925B2
Source datasetuspto-grants-2012_01
ORD IDord-df8bbd7be9c74a3ba7bc0a902b0e9e2c
Source noteuspto-grants-2012_01