4-Iodoaniline → [2-(4-Iodophenylcarbamoyl)ethyl]carbamic acid tert-butyl ester
反応式
[I:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.[C:9]([O:13][C:14]([NH:16][CH2:17][CH2:18][C:19](O)=[O:20])=[O:15])([CH3:12])([CH3:11])[CH3:10].Cl.CN(C)CCCN=C=NCC.ON1C2N=CC=CC=2N=N1>CN(C=O)C>[C:9]([O:13][C:14](=[O:15])[NH:16][CH2:17][CH2:18][C:19](=[O:20])[NH:6][C:5]1[CH:7]=[CH:8][C:2]([I:1])=[CH:3][CH:4]=1)([CH3:12])([CH3:10])[CH3:11]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of 4-iodoaniline (2.0 g, 9.17 mmol), 3-tert-butoxycarbonylaminopropionic acid (1.61 g, 8.49 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.95 g, 10.19 mmol), 1-hydroxy-7-azabenzotriazole (0.12 g, 0.85 mmol), and DMF (20 mL), was stirred at room temperature for 72 hours. The solvent was evaporated in vacuo. The residue was dissolved in methylene chloride (100 mL) and washed with 10% citric acid (2×50 mL), then 10% aqueous K2CO3 (2×50 mL). The organic layer was dried over sodium sulfate and evaporated in vacuo. The residue was purified by flash chromatography (silica gel, 3:1, v/v hexanes/ethyl acetate, then 1:1 hexanes/ethyl acetate) to provide 310 (2.44 g, 69%). 1H NMR (300 MHz, CDCl3) δ 1.44 (s, 9H), 2.60 (t, 2H), 3.49 (q, 2H), 7.36 (d, 2H), 7.60 (d, 2H).
後処理
- customThe solvent was evaporated in vacuo
- dissolutionThe residue was dissolved in methylene chloride (100 mL)
- washwashed with 10% citric acid (2×50 mL)
- dry with materialThe organic layer was dried over sodium sulfate
- customevaporated in vacuo
- customThe residue was purified by flash chromatography (silica gel, 3:1, v/v hexanes/ethyl acetate
出典と根拠
- ORDレコード
- ord-456a2631cf644dd993cc24cc677d09f5
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07875619B2
反応ノート
読み込み中…