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HRID 481487作成日:2026年10月26日

(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine → (2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine dihydrochloride

https://huagongshe.com/reaction/481487

反応式

関与物質

役割名称HCID仕込み量
反応物(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidineHCID 9799042—
反応物Hydrochloride methanolHCID 21893726—
生成物(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine dihydrochlorideHCID 995459285%

反応手順

Compound 4 (89 mg, 0.25 mmol) was treated with hydrogen chloride-methanol (5 ml). After the solvent was evaporated in vacuo, the residue (pale yellow solid) was recrystallized from ethanol-diethyl ether to give Compound 5 (91 mg, 85%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05789423
出典データセットuspto-grants-1998_08
ORD IDord-f263c02321954e629af05718b16c72d2
出典メモuspto-grants-1998_08