Sodium Carbonate → HCID 86586407、化合物
反応式
[CH3:1][C@@H:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][CH2:8][C:9]1[O:10][C:11]2[CH:17]=[CH:16][C:15]([C:18]3[CH:19]=[C:20]([C:24](=O)[CH3:25])[CH:21]=[CH:22][CH:23]=3)=[CH:14][C:12]=2[CH:13]=1.Cl.[NH2:28][OH:29].C([O-])([O-])=O.[Na+].[Na+]>CO>[CH3:1][C@@H:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][CH2:8][C:9]1[O:10][C:11]2[CH:17]=[CH:16][C:15]([C:18]3[CH:19]=[C:20]([C:24](=[N:28][OH:29])[CH3:25])[CH:21]=[CH:22][CH:23]=3)=[CH:14][C:12]=2[CH:13]=1参加物
実験手順
The product from Example 136C (240 mg, 0.5 mmol) and hydroxylamine hydrochloride (139 mg, 2.00 mmol) were dissolved into methanol (2 mL) and treated with Na2CO3 (318 mg, 3.0 mmol). The suspension was stirred at room temperature overnight and then heated at 70° C. three days. The mixture was cooled to room temperature and filtered, the solids being rinsed with 50% MeOH/CH2Cl2. The filtrate was concentrated, then partitioned between water and MeOH/CH2Cl2; some clean product remained undissolved and was separated. The organic phase was concentrated, dissolved in a little methanol, and seeded with the previously collected product. After this material had crystallized, both crops of product were rinsed with methanol and permitted to dry to provide the title compound as a white microcrystalline solid (49% yield). 1HNMR (300 MHz, CDCl3) δ 1.18 (d, 3H), 1.4-2.1 (m, 4H), 2.2-2.6 (m, 3H), 2.34 (s, 3H), 3.00-3.12 (m, 2H), 3.20-3.34 (m, 2H), 6.49 (s, 1H), 7.41-7.48 (m, 3H), 7.56-7.63 (m, 2H), 7.68 (dd, 1H), 7.70 (bs, 1H), 7.88 (dd, 1H).
後処理
- temperatureheated at 70° C. three days
- temperatureThe mixture was cooled to room temperature
- filtrationfiltered
- washthe solids being rinsed with 50% MeOH/CH2Cl2
- concentrationThe filtrate was concentrated
- custompartitioned between water and MeOH/CH2Cl2
- customwas separated
- concentrationThe organic phase was concentrated
- dissolutiondissolved in a little methanol
- customAfter this material had crystallized
- washboth crops of product were rinsed with methanol
- customto dry
出典と根拠
- ORDレコード
- ord-0e3f0333cb8a4d9ca7d3380facad71aa
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07538138B2
反応ノート
読み込み中…