Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 86651466 | HCID 86651466 | — |
| Reactant | HCID 86651468 | HCID 86651468 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 86651464 | HCID 86651464 | — |
Reaction Steps
To a stirring mixture of 6,6-dimethyl-5-((1E,3E)-4-(N-phenylacetamido)buta-1,3-dienyl)-1,2,3,6-tetrahydropyrrolo[3,2,1-ij]quinolinium-7-sulfonate and 6-(5-carboxypentyl)-5,6-dimethyl-1,2,3,6-tetrahydropyrrolo[3,2,1-ij]quinolinium-7-sulfonate in 5 mL acetic anhydride was added 5 mL pyridine. The reaction was heated to 110° C. for 2 hours. After cooling to room temperature the product was precipitated with ethyl acetate, washed with Et2O, and isolated by vacuum filtration. The final product was purified by reverse-phase HPLC yielding a blue solid. MS m/z calculated for C36H43N2O8S2 (M+H): 695.25. Found 695.3 (M+H, ESI+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309059B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-09b52f050e7f4189a3f809a4c90432d8 |
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| Source note | uspto-grants-2012_11 |
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