HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568172Generated: October 30, 2026
Hydrochloric Acid → 3-(4-Pyridyl)-2-(4-fluorophenyl)-4,7-diaza-indole
https://huagongshe.com/reaction/568172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | HCID 10991586 | HCID 10991586 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Pyridyl)-2-(4-fluorophenyl)-4,7-diaza-indole | HCID 18175225 | — |
Reaction Steps
1-(4-Fluorophenyl)-2-t-butyldimethylsiloxy-2-(4-pyridyl) ethanone (16) (5.44 g, 15.77 mmol), 2-aminopyrazine (1.00 g, 10.5 mmol), and concentrated HCl (30 mL) were heated in a sealed tube to 190° C. behind an explosion shield. After 3 h at 190° C., the reaction was allowed to cool to 23° C. then diluted with water (100 mL). After further dilution with concentrated ammonium hydroxide to pH of 12, the reaction was extracted with methylene chloride (3×200 mL), and dried (MgSO4). After concentration in vacuo, the residue was purified by applying flash chromatography (100% ethyl acetate) to afford 3-(4-pyridyl)-2-(4-fluorophenyl)-4,7-diaza-indole (62): Mass Spectrum (CI) 291 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180643B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-5d5e05f8dece462fb3452c314609db7b |
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| Source note | uspto-grants-2001_01 |
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