Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11396607 | HCID 11396607 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44434818 | HCID 44434818 | 48% |
Reaction Steps
To a solution of Example 75 (6 mg, 0.013 mmol) in THF (200 μl) at 0° C. was added Et3N (3 μl, 0.021 mmol) followed by the acetic anhydride (5 μl, 0.04 mmol). The reaction mixture was stirred at 0° C. for 5 minutes and then at rt for 10 minutes. The solvent was evaporated under pressure, and the residue was purified by preparative HPLC using 0 to 100% B over 10 minutes (Column, Luna 10μ, C18 25×100 mm; Solvent A, 10% ACN +90% H2O with 0.1% TFA; Solvent B, 90% ACN+10% H2O with 0.1% TFA) to afford the title compound (2.8 mg, 48%) as a white lyophilite. MS m/z 486 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205318B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-e4139c06e57147a29055b4c21359de1c |
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| Source note | uspto-grants-2007_04 |
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