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HRID 12860作成日:2026年10月25日

Piperidin-4-ol → tert-Butyl-5-(4-hydroxy-piperidin-1-yl)-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/reaction/12860

反応式

関与物質

役割名称HCID仕込み量
反応物Piperidin-4-olHCID 79341—
反応物1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 25014417—
生成物tert-Butyl-5-(4-hydroxy-piperidin-1-yl)-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 25014419—

反応手順

Heating a mixture of 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (Example 36, 101 mg; 0.30 mmol) and piperidin-4-ol (303 mg; 3.0 mmol) under microwave irradiation according to the procedure described in Example 37, Step 5 provided after purification by reverse phase HPLC, 1-tert-butyl-5-(4-hydroxy-piperidin-1-yl)-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (14 mg, 12%) as an off-white powder. ES-HRMS m/e calcd for C23H37N4O2 (M+H+) 357.2649, found 357.2650.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-113615d721cf4c3f8fe8c9b69c2ebafd
出典メモuspto-grants-2010_06