HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090780Generated: October 30, 2026
Sodium Bicarbonate → HCID 66974757, compound
https://huagongshe.com/reaction/2090780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | HCID 66974708 | HCID 66974708 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66974757 | HCID 66974757 | — |
Reaction Steps
To a solution (2 mL) of tert-butyl {[5-(4-cyanophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate (382 mg) in ethyl acetate was added a 4 mol/L hydrogen chloride-ethyl acetate solution (3 mL) at room temperature. The mixture was stirred for 3 hr, and basified with a saturated aqueous sodium hydrogencarbonate solution. The mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane-ethyl acetate=1:1→1:9) to give a free salt of the title compound as a pale-yellow oil. The obtained free salt was dissolved in ethyl acetate, and added to a solution (2 mL) of fumaric acid (77.1 mg) in methanol. The solvent was evaporated under reduced pressure, and the residue was recrystallized from a mixed solvent of ethanol and water to give the title compound as colorless crystals (yield 218 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436187B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-fc1fef2552024b7a95efe5478f42d85f |
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| Source note | uspto-grants-2013_05 |
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