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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655854생성일: 2026년 10월 27일

1-Hydroxybenzotriazole → 1-Methyl-1H-imidazole-2-carboxylicacid[4-(4-amino-pyrazolo[3,4-d]pyrimidin-1-yl)-phenyl]-amide

https://huagongshe.com/reaction/655854

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-methyl-1H-imidazole-2-carboxylic acidHCID 557678—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-(4-Amino-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamineHCID 11995960—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물1-Methyl-1H-imidazole-2-carboxylicacid[4-(4-amino-pyrazolo[3,4-d]pyrimidin-1-yl)-phenyl]-amideHCID 1199654835%

반응 단계

Title compound 11A, 1-(4-amino-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine (30 mg, 1.1 eq, 0.13 mmol) was added to a solution 1-methyl-1H-imidazole-2-carboxylic acid (15 mg, 1.0 eq, 0.12 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (20 mg, 1.1 eq, 0.13 mmol), 1-hydroxybenzotriazole (16 mg, 1.0 eq, 0.12 mmol) in DMF (1 ml) which had been stirred for 10 minutes under an inert atmosphere. The reaction was stirred at room temperature for 18 hours, after which methanol (1 ml) was added, and the solvents were removed in vacuo. The residue was then triturated with methanol and the resultant solid was isolated by filtration to yield the title compound as a yellow solid (14 mg, 0.04 mmol, 35%). LCMS: [M+H]+=335, Rt=1.44 min, 100% purity.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071607B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-ce593ae4affc466cbb058f9afd58c033
출처 메모uspto-grants-2011_12