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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642291Generated: October 30, 2026

Sodium hydride → HCID 68427417, compound

https://huagongshe.com/reaction/642291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-((tert-butoxycarbonyl)amino)acetateHCID 357729—
ReactantHCID 58610288HCID 58610288—
SolventDimethylformamideHCID 6228—
ProductHCID 68427417HCID 6842741732.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-bromomethyl-2-(4-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester (2.22 g, 6.18 mmol), tert-butoxycarbonylamino-acetic acid ethyl ester (1.32 g, 6.48 mmol) and sodium hydride (60% in mineral oil, 296 mg, 7.4 mmol) in anhydrous dimethylformamide (30 mL) was stirred at 0° C. for one hour and room temperature for four hours before it was quenched with brine. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a yellow oil (964 mg): 1H NMR (CDCl3, 200 MHz): δ=7.87 (d, 2H), 7.39 (d, 2H), 4.99 (m, 2H), 4.21 (m, 6H), 1.45 (s, 9H), 1.26 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-843de80454ca4fa3923b552e7a005a17
Source noteuspto-grants-2010_04