HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395743Generated: October 25, 2026
Phosphoric Acid → 1-[3-(1,1-Dimethylethylamino)pyridyl]piperazine
https://huagongshe.com/reaction/2395743
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | tert-Butyl 4-(3-aminopyridin-2-yl)piperazine-1-carboxylate | HCID 2756375 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[3-(1,1-Dimethylethylamino)pyridyl]piperazine | HCID 11042683 | — |
Reaction Steps
Isobutylene (10 ml) is condensed into a solution of 1-[1,1-dimethylethoxycarbonyl]-4-[3-amino-2-pyridinyl]piperazine (International Publication No. WO 88/08424, 200 mg) in methylene chloride (10 ml) at -70°. Phosphoric acid (85%, 50 μl) is added and the mixture stirred for 60 minutes. Boron trifluoride etherate (200 μl) is added dropwise and the resulting suspension is stirred 8 hours at reflux and overnight at 20°-25° allowing the isobutylene to evaporate. The suspension is diluted with water and ammonium hydroxide is added until basic to pH paper and then extracted with methylene chloride (3 ×). The combined extracts are dried over anhydrous potassium carbonate, filtered, and concentrated under reduced pressure to a liquid which is flash chromatographed (silica gel, 230-400 mesh), eluting with methanol/chloroform (3/20). The appropriate fractions are pooled and concentrated to give an oil. The NMR, CMR, IR, and MS (m/e) M+234 support the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05489593 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-018b339dcfa24b7e9115828dc43d6d41 |
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| Source note | uspto-grants-1996_02 |
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