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HRID 217172作成日:2026年10月25日

Trifluoroacetic acid → 2-(3-Piperidin-4-ylmethyl-[1,2,4]oxadiazol-5-yl)furo[3,2-c]pyridine

https://huagongshe.com/reaction/217172

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物4-(5-Furo[3,2-c]pyridin-2-yl-[1,2,4]oxadiazol-3-ylmethyl)piperidine-1-carboxylic acid tert-butyl esterHCID 57659562—
溶媒DichloromethaneHCID 6344—
生成物2-(3-Piperidin-4-ylmethyl-[1,2,4]oxadiazol-5-yl)furo[3,2-c]pyridineHCID 11630584—

反応手順

TFA (10 mL) was added to a stirred solution of 4-(5-furo[3,2-c]pyridin-2-yl-[1,2,4]oxadiazol-3-ylmethyl)piperidine-1-carboxylic acid tert-butyl ester (Example 44, 1.76 g, 4.56 mmol) in anhydrous CH2Cl2 (20 mL). After 1 h, the solvents were removed under reduced pressure. The residue was taken up in CH2Cl-MeOH (9:1, 100 mL), before being washed with 2M NaOH (100 mL). The aqueous phase was extracted with CH2Cl2-MeOH (9:1, 2×100 mL), then the organic extracts were combined, dried (MgSO4), and concentrated to furnish the title compound: m/z (ES+)=285.0 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193359B2
出典データセットuspto-grants-2012_06
ORD IDord-de6df570550149789450fbf124e1e1c2
出典メモuspto-grants-2012_06