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HRID 23208作成日:2026年10月26日

Hydrochloric Acid → Methyl 4-Boc-piperazine-2-acetate

https://huagongshe.com/reaction/23208

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
反応物Methyl 2-(1,4-dibenzylpiperazin-2-yl)acetateHCID 22710010—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物Methyl 4-Boc-piperazine-2-acetateHCID 275681676.4%

反応手順

The 13.7 g (40 mmol) of methyl 1,4-dibenzylpiperazine-2-acetate, 150 mL of MeOH, 50 mL of 1 N HCl (aqueous) and 3 g of 10% Pd/C were combined and hydrogenated with H2 (50 psi) for 24 hours. The reaction was filtered, the filtrate was concentrated in vacuo to remove most of the MeOH, and the residue was made basic with K2CO3 to pH=9-10, and 9.8 g (40 mmol) of BOC-ON was added slowly at 0° C. The reaction was stirred at 0° for 1 hour, allowed to warm up to room temperature, stirred for 2 hours, and extracted with ethyl acetate (2×200 mL). The combined extracts were treated with 50 mL of 10% HCl (aqueous). The aqueous layer was washed with ethyl acetate, basified with K2CO3 and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 7.89 g of methyl 4-Boc-piperazine-2-acetate; 1H NMR (CDCl3) δ 1.4 (s,9), 2.31 (dd,1), 2.37 (dd, 1), 2.55 (b, 1), 2.69-3.02 (m,4), 3.75 (s,3), 3.88 (b, 2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849739B2
出典データセットuspto-grants-2005_02
ORD IDord-a859f4b242f8477099a02a6606c472aa
出典メモuspto-grants-2005_02