HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276780Generated: October 30, 2026
Acetic Acid → 2-(4-Isopropylpiperazin-1-yl)isonicotinonitrile
https://huagongshe.com/reaction/276780
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-(Piperazin-1-yl)pyridine-4-carbonitrile | HCID 16227986 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Isopropylpiperazin-1-yl)isonicotinonitrile | HCID 18671525 | 59% |
Reaction Steps
To a solution of 2-piperazin-1-yl-isonicotinonitrile (10 g, 53 mmol), glacial acetic acid (4.26 ml, 4.5 g, 74.4 mmol, 1.4 equiv) and acetone (4.29 ml, 3.39 g, 58 mmol, 1.1 equiv) in anhydrous dichloromethane was added sodium triacetoxyborohydride (13.5 g, 63.8 mmol, 1.2 equiv). The reaction was stirred overnight, then an aqueous solution of 1 N NaOH solution was added (150 ml) and the mixture was extracted once with dichloromethane, then twice with a solution of 10% methanol/dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Purification of the residue by flash column chromatography (5% methanol/CH2Cl2 grading to 10% methanol/CH2Cl2) provided the desired product (6.52 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355635B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-e14bb971f8be4335955395148d3cd03f |
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| Source note | uspto-grants-2002_03 |
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