HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471607Generated: October 30, 2026
Pyridine → 6-Chloro-2-isobutylamino-nicotinonitrile
https://huagongshe.com/reaction/1471607
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Chloro-2-isobutoxy-nicotinamide | HCID 57968959 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Chloro-2-isobutylamino-nicotinonitrile | HCID 86636471 | 91% |
Reaction Steps
To a solution of 6-chloro-2-isobutoxy-nicotinamide (3, 2.39 g, 10.4 mmol) in acetonitrile (anhydrous, 150 mL) were added pyridine (6.75 mL, 83.5 mmol) and POCl3 (3.82 mL, 41.7 mmol). The reaction was heated at 55° C. for 3 hours. After cooling to room temperature, NaOH solution (10% aq.) was slowly added till pH 9. EtOAc (60 mL) was added and the layers separated. The aqueous layer was extracted with EtOAc (2×60 mL). The combined organic layer was dried over MgSO4, filtered, and concentrated in vacuo. Purification was accomplished by silica gel chromatography, eluting with 2%-30% EtOAc/hexanes gradient, to afford 2 g (91% yield) of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012431B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-d2d0ccb77398477f8d337e5f1c3d1009 |
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| Source note | uspto-grants-2015_04 |
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