HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362892Generated: November 1, 2026
Ammonium Acetate → HCID 67594506, compound
https://huagongshe.com/reaction/362892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 67596517 | HCID 67596517 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67594506 | HCID 67594506 | 49.9% |
Reaction Steps
Step 4): Sodium cyanoborohydride (0.06 g, 9.5 mmol) was added to solution of 2-[2-(4-oxopiperidin-1-yl)ethyl]thio-4,5-diphenylimidazole (0.34 g, 0.91 mmol), powdered 3A molecular sieves (0.268 g) and ammonium acetate (0.73 g, 9.5 mmol) in methanol (10 ml). The mixture was stirred at room temperature under nitrogen atmosphere for 65 hours and then filtered and washed with methanol. The filtrate was concentrated. The residue was dissolved in 10% NaOH solution and ethyl acetate. The organic layer was washed with water and saturated NaCl solution, dried (MgSO4) and concentrated. The residue was purified by column chromatography on silica gel (0.8% NH4OH in chloroform/methanol) to give 2-[2-(4-aminopiperidin-1-yl)ethyl]thio-4,5-diphenylimidazole (172 mg, 49.9%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05872115 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-763ddb93ac924736abcffd85e84b3bd2 |
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| Source note | uspto-grants-1999_02 |
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