HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842669Generated: October 30, 2026
Trimethylamine oxide → HCID 22614849, compound
https://huagongshe.com/reaction/842669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylamine oxide | HCID 1145 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | HCID 22614845 | HCID 22614845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22614849 | HCID 22614849 | 73% |
Reaction Steps
9-Borabicyclo[3.3.1]nonane (0.5M in tetrahydrofuran, 9.1 mL, 4.55 mmol) was added dropwise to a stirred suspension of 6,7-dichloro-2,3-dimethoxy-5-(1-allyl-1H-tetrazol-5-yl)quinoxaline (Preparation 19, 0.67 g, 1.82 mmol) in dry tetrahydrofuran (15 mL) at room temperature under nitrogen. The reaction mixture was heated under reflux for 18 hours, trimethylamine-N-oxide (1.03 g, 13.7 mmol) was added portionwise to the cooled reaction mixture and the mixture was heated under reflux for 2 hours then concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, by gradient elution using dichloromethane:methanol (100:0 changing to 99.5:0.5, by volume) to give the title compound (0.510 g, 73%) as a white solid, mp 188-189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376490B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-fa021e5af5ac46ef94633a3e0e33e9c6 |
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| Source note | uspto-grants-2002_04 |
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