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HRID 656957作成日:2026年10月26日

Acetonitrile → Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate

https://huagongshe.com/reaction/656957

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Potassium CarbonateHCID 11430—
反応物benzyl N-(2-bromoethyl)carbamateHCID 278694—
反応物4-(N-Boc-amino)piperidineHCID 723833—
溶媒DimethylformamideHCID 6228—
生成物Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamateHCID 2298997693.3%

反応手順

A mixture of phenylmethyl (2-bromoethyl)carbamate (12.9 g, 50 mmol) (prepared from phenylmethyl (2-bromoethyl)carbamate and phenylmethyl chloridocarbonate according to the method of A. J. Brouwer and R. M. J. Liskamp, European Journal of Organic Chemistry (2005), (3), 487-495), 1,1-dimethylethyl 4-piperidinylcarbamate (10 g, 50 mmol), potassium carbonate (6.9 g, 50 mmol), acetonitrile (100 ml) and DMF (30 ml) was heated at 40° C. for 2.5 days. The solvents were decanted from inorganic residues and evaporated. The residue was partitioned between ethyl acetate and dilute brine. The organic extract was dried (MgSO4) and evaporated affording a white solid (17.6 g, 93%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071592B2
出典データセットuspto-grants-2011_12
ORD IDord-2be4e431668143509c580027eb637861
出典メモuspto-grants-2011_12