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HRID 1077作成日:2026年10月23日

Phthalimide → Phenylmethyl 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1-piperidinecarboxylate

https://huagongshe.com/ja/reaction/1077

反応式

関与物質

役割名称HCID仕込み量
反応物PhthalimideHCID 6809—
反応物TriphenylphosphineHCID 11776—
反応物Benzyl piperidine-1-carboxylateHCID 228749—
反応物Diethyl azodicarboxylateHCID 5462977—
溶媒TetrahydrofuranHCID 8028—
生成物Phenylmethyl 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1-piperidinecarboxylateHCID 2183110550%

反応手順

A solution of DEAD (1.61 mL, 10.2 mmol) in 20 mL of THF was added to a solution of triphenylphosphine (2.69 g, 10.3 mmol), the N-Cbz-piperidine prepared in Example 16A (2.36 g, 100 mmol) and phthalimide (1.50 g, 10.2 mmol) in 80 mL of THF. After stirring 10.5 h at R.T. the mixture was quenched with water, extracted with EtOAc (3×) and the combined extracts washed with brine solution, dried over Na2SO4 and concentrated to give the crude product. Purification of this material by chromatography (hexanes/EtOAc; 2:1) gave 1.81 g, (50%) of 1-benzyloxycarbonyl-4-phthalimidylpiperidine. [1H]-NMR(CDCl3) consistent with structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723490
出典データセットuspto-grants-1998_03
ORD IDord-d13c6a79a6d1480ca22e3b132fc186d6
出典メモuspto-grants-1998_03