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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117955Generated: 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/2117955

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 numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-af6eeb699df54d2fb06da7fe84513fee
Source noteuspto-grants-2008_10