Acetic Anhydride → HCID 67973349、化合物
反応式
[C:1]([O:4]C(=O)C)(=[O:3])[CH3:2].[F:8][C:9]1[CH:10]=[C:11]([C:19]2[C:20]([CH3:34])=[CH:21][C:22]([O:25][CH2:26][C:27]([CH3:33])([CH3:32])[C:28]([O:30][CH3:31])=[O:29])=[N:23][CH:24]=2)[CH:12]=[CH:13][C:14]=1[C:15](=[NH:18])[NH:16]O>C(O)(=O)C>[C:1]([OH:4])(=[O:3])[CH3:2].[C:15]([C:14]1[CH:13]=[CH:12][C:11]([C:19]2[C:20]([CH3:34])=[CH:21][C:22]([O:25][CH2:26][C:27]([CH3:32])([CH3:33])[C:28]([O:30][CH3:31])=[O:29])=[N:23][CH:24]=2)=[CH:10][C:9]=1[F:8])(=[NH:16])[NH2:18]参加物
実験手順
Acetic anhydride (1.62 mL) was added to an acetic acid (10 mL) solution containing methyl 3-({5-[3-fluoro-4-(N-hydroxycarbamimidoyl)phenyl]-4-methylpyridin-2-yl}-oxy)-2,2-dimethylpropanoate (3.65 g), and the mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in methanol (30 mL), 10% palladium carbon (50%, 365 mg) was added to the resulting solution, and the mixture was stirred under hydrogen atmosphere at room temperature for 13 hours. The catalyst was filtered off by using a membrane filter, and the filtrate was concentrated under reduced pressure. Ether was added to the obtained residue, and the precipitated solid was collected by filtration, washed with ether and dried to obtain methyl 3-{[5-(4-carbamimidoyl-3-fluorophenyl)-4-methylpyridin-2-yl]oxy}-2,2-dimethylpropanoate acetic acid salt (2.45 g).
後処理
- concentrationThe reaction mixture was concentrated under reduced pressure
- dissolutionThe residue was dissolved in methanol (30 mL)
- addition10% palladium carbon (50%, 365 mg) was added to the resulting solution
- stirringthe mixture was stirred under hydrogen atmosphere at room temperature for 13 hours
- filtrationThe catalyst was filtered off
- filtrationfilter
- concentrationthe filtrate was concentrated under reduced pressure
- additionEther was added to the obtained residue
- filtrationthe precipitated solid was collected by filtration
- washwashed with ether
- customdried
出典と根拠
- ORDレコード
- ord-1415e56ea5d4457d9727dcbf662d8200
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09302996B2
反応ノート
読み込み中…