Hydrochloric Acid → 1,2,4-Pyrrolidinetricarboxylic acid, 1-(1,1-dimethylethyl) 2,4-dimethyl ester, (2S,4S)-
反応式
[C:1]([C@@H:3]1[CH2:7][N:6]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[C@H:5]([C:15]([O:17][CH3:18])=[O:16])[CH2:4]1)#N.Cl.[C:20](OC(OC(C)(C)C)=O)(OC(C)(C)C)=[O:21].C[OH:36]>>[N:6]1([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:7][C@@H:3]([C:1]([O:21][CH3:20])=[O:36])[CH2:4][C@H:5]1[C:15]([O:17][CH3:18])=[O:16]参加物
実験手順
To a solution of (2S,4S)-1-tert-butyl 2-methyl 4-cyanopyrrolidine-1,2-dicarboxylate (9.0 g, 35.4 mmol) in MeOH (196 mL) was added HCl (4M in 1,4-dioxane, 100 mL, 403 mmol). The solution was stirred at room temperature for 16h and concentrated in vacuo. The crude intermediate was dissolved in EtOAc (180 mL) and basified with aqueous bicarbonate (sat.). Di-tert-butyl dicarbonate (8.5 g, 38.9 mmol) was added and the biphasic solution was stirred at room temperature for 12h. The layers were then separated and the aqueous layer was backextracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated. The crude oil was purified by silica gel chromatography (15% to 40% to 100% EtOAc/Hexanes) to provide (2S,4S)-1-tert-butyl 2,4-dimethyl pyrrolidine-1,2,4-tricarboxylate (9.56 g, 94%).
後処理
- concentrationconcentrated in vacuo
- dissolutionThe crude intermediate was dissolved in EtOAc (180 mL)
- customThe layers were then separated
- washThe combined organic layers were washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe crude oil was purified by silica gel chromatography (15% to 40% to 100% EtOAc/Hexanes)
出典と根拠
- ORDレコード
- ord-b0b69ff99f844f4181fc166bf205bee4
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09221833B2
反応ノート
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