Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246543Generated: October 27, 2026

Water → tert-Butyl{2-[(4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl)amino]ethyl}carbamate

https://huagongshe.com/reaction/1246543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
ReactantN-{4-[2-(4-aminophenyl)ethyl]thiazol-2-yl}acetamideHCID 21914814—
SolventTolueneHCID 1140—
Producttert-Butyl{2-[(4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl)amino]ethyl}carbamateHCID 86595614—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of N-{4-[2-(4-aminophenyl)ethyl]-1,3-thiazol-2-yl}acetamide (100 mg) in toluene were added tert-butyl (2-bromoethyl)carbamate (87.5 mg) and N,N-diisopropylethylamine (52 μl), and the mixture was stirred at 80° C. for 24 h. The reaction mixture was allowed to cool to room temperature, water (10 ml) was added, and the organic layer was separated, washed with saturated aqueous NaCl, dried over MgSO4, filtered, and concentrated in vacuo to give tert-butyl {2-[(4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl)amino]ethyl}carbamate as a pale brown amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125901B2
Source datasetuspto-grants-2006_10
ORD IDord-ad1f7313227546a1b3d5980f52eff474
Source noteuspto-grants-2006_10