HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 136054475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 136054509 | HCID 136054509 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136054475 | HCID 136054475 | 79% |
Reaction Steps
To a suspension of N-[(4′-{[2-(hydroxyamino)-3-methylbutyl]sulfonyl}biphenyl-3-yl)methyl]-4-oxo-3,4-dihydroquinazoline-2-carboxamide obtained in Reference Example 107 (0.100 g, 0.192 mmol) and acetic acid (2 mL) in THF (20 mL) was added acetic anhydride (0.018 mL, 0.192 mmol) at room temperature, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was crystallized from EtOH-ethyl acetate-diethyl ether-hexane to give the title compound as a white powder (0.085 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915267B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-65fabcff6bee4ce4a8d16097b6a07316 |
| Source note | uspto-grants-2011_03 |