Imidazole → 1,1-dimethylethyl (4R)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-iodopentanoate
反応式
[CH3:1][C:2]([O:5][C:6]([NH:8][C@@H:9]([CH2:19]O)[CH2:10][CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])=[O:7])([CH3:4])[CH3:3].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.[I:45]I>C(Cl)Cl>[CH3:1][C:2]([O:5][C:6]([NH:8][C@@H:9]([CH2:19][I:45])[CH2:10][CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])=[O:7])([CH3:4])[CH3:3]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of crude 1,1-dimethylethyl (4R)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-hydroxypentanoate (23.8 g, 82.4 mmol), triphenylphosphine (32.42 g, 123.6 mmol) and imidazole (8.41 g, 123.6 mmol) in 515 mL anhydrous CH2Cl2 under N2 at 0° C. was added iodine over 15 min portionwise. The ice bath was removed, and the reaction was allowed to warm to room temperature and stirred over 30 min. The reaction was quenched with 200 mL H2O, and the aqueous layer was extracted with diethyl ether (2×150 mL). The combined organic layers were washed with sat. aq. Na2SO3 solution (2×25 mL) and brine (25 mL), dried over MgSO4, and concentrated in vacuo. Purification of the residue by silica gel chromatography (Analogix IF280, 5% -50% EtOAc/Hex) afforded the title compound as a white solid (25.34 g, 77%). ESMS [M+H]+=400.4.
後処理
- customThe ice bath was removed
- customThe reaction was quenched with 200 mL H2O
- extractionthe aqueous layer was extracted with diethyl ether (2×150 mL)
- washThe combined organic layers were washed with sat. aq. Na2SO3 solution (2×25 mL) and brine (25 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customPurification of the residue by silica gel chromatography (Analogix IF280, 5% -50% EtOAc/Hex)
出典と根拠
- ORDレコード
- ord-435a615a99b44528b1ae01ee6f05b324
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07582668B2
反応ノート
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