HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168253Generated: November 1, 2026
Diethyl cyanophosphonate → 5-amino-6-chloro-2-ethyl-N-(piperidin-4-ylmethyl)imidazo[1,2-a]pyridine-8-carboxamide
https://huagongshe.com/reaction/1168253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| Reactant | 5-Amino-6-chloro-2-ethylimidazo[1,2-a]pyridine-8-carboxylic acid | HCID 22236496 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-amino-6-chloro-2-ethyl-N-(piperidin-4-ylmethyl)imidazo[1,2-a]pyridine-8-carboxamide | HCID 9949612 | 90% |
Reaction Steps
A mixture of 5-amino-6-chloro-2-ethylimidazo[1,2-a]pyridine-8-carboxylic acid (EXAMPLE 10, Step 2, 10.00 g, 41.72 mmol), tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (J. Prugh, L. A. Birchenough and M. S. Egbertson, Synth. Commun., 1992, 22, 2357-60) (15.20 g, 70.93 mmol), diethyl phosphorocyanidate (10.76 mL, 70.93 mmol) and diisopropylethylamine (18.17 mL, 104.4 mmol) in N,N-dimethylformamide (267 mL) was stirred at room temperature for 43 h. The solvent was removed by evaporation. The residue was basified with aqueous sodium bicarbonate (40 mL), and extracted with dichloromethane (5×100 mL). The combined extract was washed with brine, dried over magnesium sulfate, and concentrated in vacuo. Flash chromatography of the residue eluting with dichloromethane/methanol (100:1 to 20:1) afforded 19.08 g (90%) of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06624162B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-3d0e74c1d1c2417b8ded164c643c1665 |
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| Source note | uspto-grants-2003_09 |
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