HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436204Generated: October 30, 2026
Acetyl chloride → 1-Ethyl-2-methyl-5,6-diphenyl-1H-imidazo[4,5-b]pyrazine
https://huagongshe.com/reaction/436204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-N-ethyl-5,6-diphenyl-2-pyrazinamine | HCID 21454804 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Ethyl-2-methyl-5,6-diphenyl-1H-imidazo[4,5-b]pyrazine | HCID 21454790 | — |
Reaction Steps
2-Chloro-3-ethylamino-5,6-diphenylpyrazine, (3.10 g, 0.01 moles) is dissolved in benzene (50 ml) and then triethylamine (1.29 g, 0.013 moles) and acetyl chloride (1.00 g, 0.013 moles) are added. The solution is refluxed 41/2 hours, cooled to 15° C and filtrate. The filtrate is diluted with ethanol (3 ml), warmed briefly at 50° C and then all volatile materials evaporated. The resultant brown oil is treated with liquid ammonia (17 g) in ethanol (60 ml) in a bomb at 165° C for 12 hours. The solution is diluted with water (200 ml), cooled and the yellow precipitate filtered off. The solid is triturated with boiling 50% aqueous methanol, filtered, and the filtrate chilled. The product is collected by filtration. Yield 0.45 g (14%). It is recrystallized from benzene-heptane, m.p. 178.5°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04007170 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-b5b1e2cf8de0479fa06be2ab4f999950 |
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| Source note | uspto-grants-1977_02 |
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