Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060240Generated: October 26, 2026

Potassium Carbonate → Tert-butyl 2-[(2-acetamido-1,3-thiazol-5-yl)sulfanyl]acetate

https://huagongshe.com/reaction/1060240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantD-1,4-DithiothreitolHCID 446094—
Reactant2-Acetamino-5-thiocyanatothiazoleHCID 15346341—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-[(2-acetamido-1,3-thiazol-5-yl)sulfanyl]acetateHCID 532966187%

Reaction Steps

To a mixture of 2-acetamino-5-thiocyanatothiazole (5.97 g, 30 mmol) in MeOH (360 mL) under argon was added dithiothreitol (9.26 g, 60 mmol) at rt. The mixture was stirred at rt for 2 h and it was concentrated to afford a reduced solid product. This solid product was dissolved in DMF (30 mL) and to this solution were added tert-butyl bromoacetate (5.85 g, 30 mmol) and potassium carbonate (5.0 g, 36 mmol). The mixture was stirred at rt for 2 h and water (200 mL) was added to the mixture. The precipitates were collected, washed with water and dried. The solid was dissolved in methylene chloride (100 mL) and MeOH (10 mL) and filtered through a silica gel pad. The filtrate solution was concentrated to afford the desired product (7.5 g, 87%) as a solid, mp 162-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521759B2
Source datasetuspto-grants-2003_02
ORD IDord-3ef16d6a45dd47a595ca77d268693b4c
Source noteuspto-grants-2003_02