Sodium periodate → Methyl (4-{3-cyano-4-formyl-5-[1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazol-3-yl]-2-thienyl}pyridin-2-yl)carbamate
反応式
[C:1]([C:3]1[C:7]([CH:8]([OH:11])CO)=[C:6]([C:12]2[N:16]=[CH:15][N:14]([CH:17]3[CH2:22][CH2:21][CH2:20][CH2:19][O:18]3)[N:13]=2)[S:5][C:4]=1[C:23]1[CH:28]=[CH:27][N:26]=[C:25]([NH:29][C:30](=[O:33])[O:31][CH3:32])[CH:24]=1)#[N:2].I([O-])(=O)(=O)=O.[Na+]>CC(C)=O.O>[C:1]([C:3]1[C:7]([CH:8]=[O:11])=[C:6]([C:12]2[N:16]=[CH:15][N:14]([CH:17]3[CH2:22][CH2:21][CH2:20][CH2:19][O:18]3)[N:13]=2)[S:5][C:4]=1[C:23]1[CH:28]=[CH:27][N:26]=[C:25]([NH:29][C:30](=[O:33])[O:31][CH3:32])[CH:24]=1)#[N:2]参加物
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
Methyl (4-{3-cyano-4-(1,2-dihydroxyethyl)-5-[1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazol-3-yl]-2-thienyl}pyridin-2-yl)carbamate (0.362 g, 0.769 mmol) was dissolved in acetone (40 mL) and water (10 mL). Sodium metaperiodate (0.494 g, 2.31 mmol) was added and the mixture was stirred at room temperature for 6 hours. Sodium metaperiodate (0.329 g, 1.54 mmol) was added and the mixture was stirred for 16 more hours. The mixture was concentrated in rotavapor. The residue was triturated with water, filtered and washed thoroughly with water, then dried in lyophilizer to give a dry solid product (0.320 g, yield 94.8%). LC/MS: (FA) ES+ 439. 1H NMR (400 MHz, d6-dmso) δ 10.67 (s, 1H), 10.57 (s, 1H), 9.05 (s, 1H), 8.49 (m, 1H), 8.28 (s, 1H), 7.50 (m, 1H), 5.69-5.73 (m, 1H), 3.94-3.98 (m, 1H), 3.73 (s, 3H), 3.66-3.71 (m, 1H), 1.93-2.12 (m, 3H), 1.58-1.71 (m, 3H).
後処理
- stirringthe mixture was stirred for 16 more hours
- concentrationThe mixture was concentrated in rotavapor
- customThe residue was triturated with water
- filtrationfiltered
- washwashed thoroughly with water
- customdried in lyophilizer
出典と根拠
- ORDレコード
- ord-1b4dc2917b954f19887ae4431cb6f862
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08796268B2
反応ノート
読み込み中…