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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32816Generated: October 25, 2026

tert-Butyl (4-(methoxy(methyl)carbamoyl)thiazol-2-yl)carbamate → tert-Butyl (4-propionylthiazol-2-yl)carbamate

https://huagongshe.com/reaction/32816

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (4-(methoxy(methyl)carbamoyl)thiazol-2-yl)carbamateHCID 58604314—
ReactantHCID 178461633HCID 178461633—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (4-propionylthiazol-2-yl)carbamateHCID 4511789755%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of ethyl magnesium chloride (126 mL, 0.252 mol, 2 M in tetrahydrofuran) was stirred and cooled to −70° C. on a dry ice/acetone bath. A solution of [4-(methoxy-methyl-carbamoyl)-thiazol-2-yl]-carbamic acid tert-butyl ester (14.5 g, 0.0504 mol) in tetrahydrofuran (200 mL) was added dropwise over approximately 5 minutes. The mixture was stirred for 1 hour. The cooling bath was removed and stirring continued for an additional 2 hours. The mixture was poured into a mixture of ice and saturated aqueous ammonium chloride solution and then extracted with ethyl acetate. The organic extracts were combined, washed with brine, dried over magnesium sulfate and evaporated to give an off white solid which was purified by chromatography over a 350 g pad of silica gel eluted with 4:1 ethyl acetate/dichloromethane to afford (4-propionyl-thiazol-2-yl)-carbamic acid tert-butyl ester (7.09 g, 55%) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427635B2
Source datasetuspto-grants-2008_09
ORD IDord-f960c4b0c9e1442295160d1539d03a1e
Source noteuspto-grants-2008_09