Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Di-tert-butyl diethylphosphoramidite | HCID 4251849 | — |
| Reactant | HCID 24771030 | HCID 24771030 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57767004 | HCID 57767004 | — |
Reaction Steps
Tetrazole (2.0 equiv., 5.37 mmol, 0.38 g) and di-(tert-butyl) diethylphosphoramidite (1.6 equiv., 4.30 mmol, 1.07 g) were added to a solution of 10 (1.0 equiv., 2.69 mmol, 1.00 g) in anhydrous acetonitrile under Ar atmosphere. The reaction mixture was stirred at room temperature for 1 h. A 70% tert-butyl hydroperoxide solution in water (5.0 equiv., 13.45 mmol, 1.73 g) was added slowly and stirring was continued for 1 h. The reaction mixture was filtered through a glass filter and the filtrate was evaporated under reduced pressure. Purification by column chromatography (dichloromethane/methanol 97.2:2.5) afforded phosphoric acid di-tert-butyl ester 6-(4-nitrophenyl)-5-oxo-5,6-dihydro-pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-9-yl ester (I21). A suspension of I21 in a 4 M HCl solution in isopropanol was stirred at room temperature overnight. The solvent was removed under reduced pressure to give phosphoric acid 5,6-dihydro-6-(4-nitrophenyl)-5-oxo-pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-9-yl ester (76) as a hydrochloride salt (0.47 g, yield=36%, purity (LC)>95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994187B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a5724ee6909a43279c8ccdde53333aad |
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| Source note | uspto-grants-2011_08 |
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