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HRID 75594作成日:2026年10月25日

Ammonia → Benzyl 4-hydrazinylpiperidine-1-carboxylate

https://huagongshe.com/reaction/75594

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 4-hydrazinylpiperidine-1-carboxylateHCID 2109831958%

反応手順

A solution of 1-CBZ-4-piperidone (2.92 g, 12.5 mmol) and hydrazine hydrate (2.01 mL, 18.8 mmol) in MeOH (25 mL) was stirred at 50° C. for 30 min, then cooled to RT and NaBH4 (1.18 g, 31.3 mmol) added (CARE: gas evolution and exotherm to −45° C.). The solution was stirred at RT for 30 min, then 50° C. for 18 h. The cooled solution was concentrated in vacuo, suspended in water (25 mL) and extracted with DCM (2×25 mL). The combined organics were passed through a hydrophobic frit and concentrated in vacuo to leave a clear oil. FCC, using 0-10% [2H NH3 in MeOH] in DCM, gave the title compound as a clear oil (1.80 g, 58%). LCMS (Method 3): Rt 2.03 min, m/z 250 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835431B2
出典データセットuspto-grants-2014_09
ORD IDord-b50190cd3b0a48b7bed0247d2c885e45
出典メモuspto-grants-2014_09