HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034594Generated: October 31, 2026
Thiophenol → 2-Amino-5-phenyl-3-phenylthiopyrazine
https://huagongshe.com/reaction/1034594
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromo-5-phenylpyrazin-2-amine | HCID 12453552 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-5-phenyl-3-phenylthiopyrazine | HCID 66848252 | 79% |
Reaction Steps
To a cooled solution of thiophenol (0.10 mL, 1.00 mmol) in dry DMF (10 mL), sodium hydride (NaH) (0.025 g, 1.00 mmol) was added the resulting mixture was stirred for 15 min at 5-10° C. After this time 2-amino-3-bromo-5-phenylpyrazine 17b (0.25 g, 1.00 mmol) was added and the mixture refluxed for 20 h, cooled and extracted with EtOAc. The organic layer was washed with water, dried over Na2SO4, filtered and the solvent removed under reduced pressure to get a crude that was purified by flash chromatography using petroleum ether-EtOAc (60:40 v/v) as eluent, to obtain 0.22 g of the title compound 18b as a brown solid (mp 109-112° C., 79% yield). 1H-NMR (CDCl3): 4.92 (br s, 2H), 7.29-7.50 (m, 8H), 7.74-7.77 (m, 2H), 8.35 (s, 1H). MS (ESI): m/z 280 (M+H1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546147B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-46b8a61e9bfe45a89f2e453e6ad3bf2a |
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| Source note | uspto-grants-2013_10 |
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