HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406181Generated: October 28, 2026
Triethylamine → 2,3-Diphenyl-5,6,7,8-tetrahydropyrido[3,2-b]pyrazine
https://huagongshe.com/reaction/406181
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3-Diphenylpyrido[2,3-b]pyrazine | HCID 817566 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Diphenyl-5,6,7,8-tetrahydropyrido[3,2-b]pyrazine | HCID 66665561 | — |
Reaction Steps
A suspension of 2,3-diphenylpyrido[3,2-b]pyrazine (Intermediate D) (49.1 g, 143 mmol), triethylamine (20 ml, 143 mmol) and 10% palladium on carbon (19.5 g) in dry THF (410 ml) was placed under an atmosphere of hydrogen (100 mbar) at room temperature for 61 h. After 24 h and 48 h additional palladium catalyst was added (2×4.9 g). The reaction mixture was filtered and the catalyst was washed with THF. The filtrate was concentrated in vacuo and the crude product was dissolved in warm EtOAc (1500 ml) and washed with sat. Na2CO3 solution (400 ml). The aqueous portion was extracted with EtOAc (200 ml) and the combined organic extracts were washed with water (150 ml), brine (300 ml), dried over sodium sulfate and concentrated in vacuo. This crude product was purified by chromatography on silica eluting with neat DCM followed by DCM (1% MeOH) to afford the title product;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754085B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-6152673d056a44cfb5847afd6b239b04 |
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| Source note | uspto-grants-2014_06 |
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