Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 69317721 | HCID 69317721 | — |
| Product | HCID 69171435 | HCID 69171435 | — |
Reaction Steps
A solution of 2-(3-chloro-4-fluorobenzyl)-10-methoxy-8-methyl-1,9-dioxo-1,2,6,7,8,9-hexahydropyrido[3′,4′:4,5]pyrrolo[1,2-a]-pyrazine-4-carboxylic acid (0.74 g, 1.70 mmol), diisopropylethylamine (0.28 g, 2.13 mmol), and diphenylphosphoryl azide (0.57 g, 2.13 mmol) in mixture of 1,2-dichlorobenzene (10 mL) and anhydrous tert-butyl alcohol (10 mL) was heated in a sealed tube in an oil bath 120° C. for one hour. The reaction mixture was concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with a methanol in ethyl acetate gradient. Collection and concentration of appropriate fractions provided the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435735B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-7e91fdb01a9e4ea8883e7278f0dce7a7 |
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| Source note | uspto-grants-2008_10 |
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