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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254073Generated: October 31, 2026

Ethyl bromoacetate → HCID 58497208, compound

https://huagongshe.com/reaction/1254073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58497238HCID 58497238—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58497208HCID 5849720857.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of Step 2 product of Example 140 (100 mg, 0.255 mmol) in THF (2 ml) at 0° C. was added NaH (20.4 mg, 0.510 mmol). After stirred at 0° C. for 1 hr, ethyl bromo acetate (0.034 ml, 0.306 mmol) was added and then stirred at 0° C. for one hour. Reaction mixture was quenched with water, extracted with EtOAc, washed with brine, dried over Na2SO4, filtered, concentrated, separated by prep. TLC (Hex:EtOAc=2:1) to give ethyl (3-{5-[(4-chlorophenyl)sulfanyl]-4-(4-cyanophenyl)-1-methyl-1H-imidazol-2-yl}-1H-pyrazol-1-yl)acetate (70 mg) desired compound. LCMS: [M+1]+=478.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455528B2
Source datasetuspto-grants-2013_06
ORD IDord-1783316d87e045b1a810162ec2b6da86
Source noteuspto-grants-2013_06