HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527967Generated: October 31, 2026
Tetrahydrofuran → HCID 86656446, compound
https://huagongshe.com/reaction/527967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Quinoxaline, 2,3-dichloro-6-fluoro- | HCID 4447681 | — |
| Reactant | HCID 12666545 | HCID 12666545 | — |
| Reactant | 1,2,2,3-Tetramethylpiperidine | HCID 18761772 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86656446 | HCID 86656446 | 71% |
Reaction Steps
A solution of tetramethylpiperidine (16.4 mL) in dry THF (100 mL) was cooled to −78° C. and treated dropwise with n-BuLi (2.5M in Hex; 39 mL). The solution was further stirred at −78° C. for 30 min. A solution of 6-fluoro-2,3-dimethoxy-quinoxaline (15.6 g; prepared from the commercially available 2,3-dichloro-6-fluoroquinoxaline according to Egyptian Journal of Chemistry (1980), Volume Date 1977, 20, 427-39) in dry THF (450 mL) was cooled to −78° C., treated dropwise with the first solution and further stirred at −78° C. for 30 min. The resulting reaction mixture was treated with DMF (11.56 mL) and further stirred at −78° C. for 15 min. The reaction mixture was poured onto a mixture of a sat. NH4Cl solution and ice and extracted with ether. The org. layer was washed with brine, dried over MgSO4, evaporated under reduced pressure and crystallised from Hex/EA affording a light yellow solid (12.5 g; 71% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346804B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-afb133ca8512465889c03faec961d0d8 |
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| Source note | uspto-grants-2016_05 |
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