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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842669Generated: October 30, 2026

Trimethylamine oxide → HCID 22614849, compound

https://huagongshe.com/reaction/842669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamine oxideHCID 1145—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantHCID 22614845HCID 22614845—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22614849HCID 2261484973%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376490B1
Source datasetuspto-grants-2002_04
ORD IDord-fa021e5af5ac46ef94633a3e0e33e9c6
Source noteuspto-grants-2002_04