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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 617228생성일: 2026년 10월 25일

Triethylamine → N-(1-Adamantyl)-5-(2-[4-morpholinyl]ethoxy)-1-(4-isopropylphenyl)pyrazole-4-carboxamide

https://huagongshe.com/reaction/617228

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium CarbonateHCID 10340—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물Amantadine HydrochlorideHCID 64150—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-(4-Isopropylphenyl)-5-(2-[4-morpholinyl]ethoxy)pyrazole-4-carboxylic acidHCID 17919400—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(1-Adamantyl)-5-(2-[4-morpholinyl]ethoxy)-1-(4-isopropylphenyl)pyrazole-4-carboxamideHCID 982699214.4%

반응 단계

To a stirred solution of 1-(4-isopropylphenyl)-5-(2-[4-morpholinyl]ethoxy)pyrazole-4-carboxylic acid (43 mg, 0.12 mmol) in dimethylformamide (1 mL) under an argon atmosphere, was added 1-hydroxybenzotriazole (16 mg, 0.12 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (25 mg, 0.13 mmol), triethylamine (60 uL, 0.43 mmol) and 1-adamantanamine hydrochloride (25 mg, 0.13 mmol). The reaction mixture was stirred for 24 h at room temperature, heated to 70° C. for 2 h, and stirred for another 96 h at room temperature. The resulting mixture was treated with aqueous sodium carbonate, extracted with ethyl acetate, washed with water four times and dried over Na2SO4. The extract was concentrated in vacuo. This coupling was repeated on the same scale and the combined residue was purified by chromatography twice over silica gel eluting the first column with 2 to 3% methanol in chloroform, and the second with 30 to 40% ethyl acetate in chloroform to afford the title compound (7% yield, 8.5 mg) as a yellow powder, mp 132-134° C. MS (ES) m/e 493.4 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05948777
출처 데이터셋uspto-grants-1999_09
ORD IDord-ef57082c3f34480bb8176acc12378372
출처 메모uspto-grants-1999_09