Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 59639565 | HCID 59639565 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59639614 | HCID 59639614 | — |
Reaction Steps
The product of Example 131 (61 mg, 0.14 mmol)was dissolved in CH2Cl2 (2 mL) and stirred at 0° C. under Ar. Triethylamine (0.1 mL) was added followed by the addition of acetic anhydride (0.2 g, 2 mmol). The reaction was allowed to slowly warm to 23° and stir for 18 h. The solvents were removed in vacuo, and the residue was flash chromatographed eluted with 10-30% EtOAc/CH2Cl2 to give the title compound as a white-amorphous solid. mp 75-79°, LC MS m/z=469 (MH+) Retention time=1.95 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314881B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-24166affeda44b0387a058c23e460381 |
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| Source note | uspto-grants-2008_01 |
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