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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271329생성일: 2026년 10월 26일

Diisopropylethylamine → (4-phenethyloxy-cyclohexyl)-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/271329

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Chloro-1H-pyrazolo[3,4-d]pyrimidineHCID 221095—
반응물HCID 178511717HCID 178511717—
용매IsopropanolHCID 3776—
생성물(4-phenethyloxy-cyclohexyl)-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)-amineHCID 1155178560%

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온도80 °C

반응 단계

A mixture of 219 mg of trans-4-(2-phenyl-ethoxy)-cyclohexylamine, 154 mg of 4-chloro-1H-pyrazolo[3,4-d]pyrimidine (R. K. Robins, J. Amer. Chem. Soc., 78, 784-790 (1956)), 10 mL of 2-propanol and 0.174 mL of N,N-diisopropyl-ethylamine was heated to 80° C. for 12 hours. The mixture was cooled and concentrated under reduced pressure and purified by either preparative TLC eluting with 50:50:5 THF:diethyl ether:NH4OH or preparative reverse phase chromatography on delta Pak C (C-18 column) eluting with a gradient of 90:10 to 0:100 of 0.1% TFA in H2O: CH3CN gave 60-92% of (4-phenethyloxy-cyclohexyl)-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)-amine as a white crystalline solid. MS (m+1)=338.32; 1H NMR (400 MHz, CDCl3) 8.43 (s, 1H), 7.92 (s, 1H), 7.3-7.2 (m, 5H), 3.7 (t, 2H), 3.3 (m, 1H), 2.9 (t, 2H), 2.22 (d, 2H), 2.1 (d, 2H), 1.7 (m, 1H), 1.5 (dd, 2H), 1.4 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452893B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-e9e6e7e07b04446583ace8012adf3970
출처 메모uspto-grants-2008_11