HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364511Generated: October 30, 2026
Ethanol → 4,6-Diamino-2-ethoxypyridine-3-carbonitrile
https://huagongshe.com/reaction/1364511
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4,6-Diamino-2-bromo-3-pyridinecarbonitrile | HCID 170668 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,6-Diamino-2-ethoxypyridine-3-carbonitrile | HCID 13149868 | 65% |
Reaction Steps
To a 5 mL sealable heavy walled glass tube suitable for microwave heating containing 5 mL of absolute ethanol was added 150 mg (6.5 mmol) of sodium metal. The mixture was stirred until all of the sodium had reacted, then 1.00 g (4.71 mmol) of 2-bromo-4,6-diaminonicotinonitrile (E. I. du Pont de Nemours and Company U.S. Pat. No. 2,790,806, 1957) was added. The tube was sealed, and the reaction was heated with a microwave apparatus at 150° C. for 10 minutes then cooled and diluted with 15 mL of water. The orange precipitate which formed was washed with water until pH=7, then dried under reduced pressure at 105° C. to provide 0.545 g (65%) of a light orange solid. 1H NMR (300 MHz, d6-DMSO) δ 6.19 (s, 2H), 6.14 (s, 2H), 5.32 (s, 1H), 4.23 (q, 2H, J=7.1 Hz), 1.25 (t, 3H, J=7.1 Hz), MS (ES) m/e=151 (M−Et+H)+, 179 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888374B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-682cdce2c8e94cce8714be14f214c135 |
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| Source note | uspto-grants-2011_02 |
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