HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264521Generated: October 30, 2026
3-Pyridinemethanol → 2-Amino-4-phenyl-6-(3-pyridinylmethoxy)-3,5-pyridinedicarbonitrile
https://huagongshe.com/reaction/2264521
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Pyridinemethanol | HCID 7510 | — |
| Reactant | 2-amino-6-chloro-4-phenylpyridine-3,5-dicarbonitrile | HCID 2786713 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-4-phenyl-6-(3-pyridinylmethoxy)-3,5-pyridinedicarbonitrile | HCID 9858576 | — |
Reaction Steps
102 mg (0.4 mmol) of 2-amino-6-chloro-4-phenyl-3,5-pyridinedicarbonitrile [Quintela et al., Heterocycles 38, 1299-1305 (1994)] and 54 mg (0.48 mmol) of potassium tert-butoxide are dissolved together in 1.696 g (=1.5 ml, 15.55 mmol) of 3-hydroxymethylpyridine, and the mixture is stirred at 60° C. for about 16 h. The resulting suspension is acidified with two drops of glacial acetic acid. The product which crystallizes out is filtered off with suction, washed with water and dried under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855219B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-705059d9258246a0b96d89126759683b |
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| Source note | uspto-grants-2010_12 |
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