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HRID 1425905作成日:2026年10月27日

Methyl iodide → 5-Benzyl 1-methyl N-(tert-butoxycarbonyl)-L-glutamate

https://huagongshe.com/reaction/1425905

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物L-Glutamic acid, N-((1,1-dimethylethoxy)carbonyl)-, 5-(phenylmethyl) esterHCID 83589—
溶媒DimethylformamideHCID 6228—
溶媒Chloroform methanolHCID 21584188—
生成物5-Benzyl 1-methyl N-(tert-butoxycarbonyl)-L-glutamateHCID 1394307082.5%

反応手順

Methyl iodide (1.01 mL, 16.3 mmol) was added dropwise to a solution of (2S)-5-(benzyloxy)-2-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acid XII (5.00 g, 14.82 mmol) and K2CO3 (2.25 g, 16.3 mmol) in DMF (25 mL) at room temperature The reaction mixture was stirred about 3 h at room temperature before adding additional methyl iodide (1.01 mL, 16.3 mmol). EtOAc was then added to the reaction and washed 3×10% Na2S2O3 and dried over MgSO4. The solvent was removed under reduced pressure and the crude product was purified on a silica gel column (100:1 and then 50:1 CHCl3/MeOH) to give 5-benzyl 1-methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}pentanedioate XIII (4.20 g, 12.23 mmol, 82% yield). ESIMS found for C18H25NO6 m/z 352 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08933018B2
出典データセットuspto-grants-2015_01
ORD IDord-4fb6be60d519414a89aa4ae48a36e745
出典メモuspto-grants-2015_01