HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351271Generated: October 29, 2026
Hydrochloric Acid → HCID 86612531, compound
https://huagongshe.com/reaction/351271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86612532 | HCID 86612532 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86612531 | HCID 86612531 | — |
Reaction Steps
A 0.76M solution of isopropyl magnesium bromide in THF (8.5 ml) was added dropwise to a solution of tert-butyl {4-[3-{[methoxy(methyl)amino]carbonyl}-1-(4-methoxy-phenyl)-1-H-pyrazol-5-yl]benzyl}carbamate (1 g) in THF (10 ml) at 10–15° C. The mixture was stirred at ambient temperature for 4 hours. The reaction mixture was poured into a mixture of 1M HCl and ice. The mixture was extracted with AcOEt. The organic layer was washed with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography eluted with AcOEt/n-hexane=20%, 25%, then 10% MeOH/CHCl3. The combined pure fraction was concentrated in vacuo to give tert-butyl {4-[3-isobutyryl-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]benzyl}carbamate (318 mg) as an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183306B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-c5b91f0159db4f668919437d35b72891 |
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| Source note | uspto-grants-2007_02 |
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