戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 12832作成日:2026年10月24日

2-Aminoadamantane hydrochloride → 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/ja/reaction/12832

反応式

関与物質

役割名称HCID仕込み量
反応物2-Aminoadamantane hydrochlorideHCID 25331—
反応物DiisopropylethylamineHCID 81531—
反応物1-tert-Butyl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 1482039—
反応物2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 2501354465%

反応手順

tert-Butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (Intermediate 7, 61 mg, 0.26 mmol) was dissolved in a mixture of dry dichloromethane (3.2 mL) and dry DMF (0.8 mL). DIPEA (0.23 mL, 1.3 mmol) and TSTU (93 mg, 0.28 mmol) were added to the above mixture. After the mixture was stirred for 1 h, the appearance of active ester was detected by LC-MS. Then 2-aminoadamantane hydrochloride (58 mg, 0.31 mmol) was added. After another 2 hours water was added and the organic layer was separated. The aqueous layer was extracted twice with dichloromethane. The combined organic layers were dried under vacuum and purified by C-18 reversed phase HPLC with a gradient of 10-100% acetonitrile/water to give 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (62 mg, 65%). Mass spectrum: m/z: 370.2 (M+1).

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-d53e24288b474cab86af0923b73f4cca
出典メモuspto-grants-2010_06