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HRID 556463作成日:2026年10月26日

Hydrochloric Acid → Rac-1-[6-chloro-3-(3-chloro-benzyl)-2-oxo-2,3-dihydro-1h-indol-3-yl]-piperidine-3-carboxylic acid

https://huagongshe.com/reaction/556463

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Nipecotic AcidHCID 4498—
反応物Sodium HydroxideHCID 14798—
反応物3-Bromo-6-chloro-3-(3-chloro-benzyl)-1,3-dihydro-indol-2-oneHCID 57507273—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物Rac-1-[6-chloro-3-(3-chloro-benzyl)-2-oxo-2,3-dihydro-1h-indol-3-yl]-piperidine-3-carboxylic acidHCID 24950102—

反応手順

To the mixture of piperidine-3-carboxylic acid (600 mg, 4.5 mmol) and NaOH (360 mg, 9 mmol) in water (5 mL) and dioxane (5 mL) was added rac-3-bromo-6-chloro-3-(3-chloro-benzyl)-1,3-dihydro-indol-2-one (1.1 g, 3 mmol). The mixture was stirred at room temperature for 1 h and then diluted by water (30 mL). The resulting solution was neutralized to pH=7 with hydrochloride acid and extracted by dichloromethane. The organic phase was dried over Na2SO4, filtered and concentrated to give rac-1-[6-chloro-3-(3-chloro-benzyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-piperidine-3-carboxylic acid yield: (0.9 g, 71%). MS: [M−H]−=417.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08058269B2
出典データセットuspto-grants-2011_11
ORD IDord-e5c6687063234747b2d042bc19b05881
出典メモuspto-grants-2011_11