HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254073Generated: October 31, 2026
Ethyl bromoacetate → HCID 58497208, compound
https://huagongshe.com/reaction/1254073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 58497238 | HCID 58497238 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58497208 | HCID 58497208 | 57.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455528B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-1783316d87e045b1a810162ec2b6da86 |
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| Source note | uspto-grants-2013_06 |
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