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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853649Generated: October 31, 2026

tert-Butyl 3-Bromothiophene-2-carbonyl[4-(tert-butyldimethylsilyloxy)phenyl]carbamate → 8-(tert-Butyldimethylsilyloxy)thieno[2,3-c]quinolin-4(5H)-one

https://huagongshe.com/reaction/1853649

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-Bromothiophene-2-carbonyl[4-(tert-butyldimethylsilyloxy)phenyl]carbamateHCID 86689440—
CatalystHCID 178418851HCID 178418851—
Product8-(tert-Butyldimethylsilyloxy)thieno[2,3-c]quinolin-4(5H)-oneHCID 67447577111.6%

Reaction Steps

Following Step 3 from General Procedure A, tert-butyl 3-bromothiophene-2-carbonyl[4-(tert-butyldimethylsilyloxy)phenyl]carbamate (1.0 g, 2.0 mmol) was reacted with bis(tri-tert-butylphosphine)palladium (50 mg, 0.098 mmol) to afford the desired product (740 mg, quant.) as a solid: ESI MS m/z 332 [C17H21NO2SSi+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962648B2
Source datasetuspto-grants-2015_02
ORD IDord-60eab21d366149db84190de6a35a27a4
Source noteuspto-grants-2015_02