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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 883053생성일: 2026년 10월 26일

1-benzyl-1H-pyrazol-3-amine → N-(1-Benzyl-1H-pyrazol-3-yl)-3-isopropoxy-5-(2-thiophen-3-yl-ethoxy)-benzamide

https://huagongshe.com/reaction/883053

반응식

참여 물질

역할이름HCID투입량
반응물1-benzyl-1H-pyrazol-3-amineHCID 1508616—
반응물3-Isopropoxy-5-(2-thiophen-3-yl-ethoxy)-benzoic acidHCID 58528913—
용매Thionyl ChlorideHCID 24386—
생성물N-(1-Benzyl-1H-pyrazol-3-yl)-3-isopropoxy-5-(2-thiophen-3-yl-ethoxy)-benzamideHCID 2526182045%

반응 조건

온도70 °C

반응 단계

3-Isopropoxy-5-(2-thiophen-3-yl-ethoxy)-benzoic acid (0.672 mmol) is dissolved in thionylchloride (1.2 ml) and heated to 70° C. for 1 hour. After cooling to room temperature, the solvent is removed in vacuo. The residue is dissolved in dichloromethane (1.2 ml) and ethyldiisopropyl-amine (167 μl) is added and 1-benzyl-1H-pyrazol-3-ylamine (1.2 eq) is added. The solution is stirred 21 hours at room temperature. The reaction solution is extracted with water. The organic layer is washed with brine and dried over MgSO4 and the solvent is removed in vacuo. N-(1-Benzyl-1H-pyrazol-3-yl)-3-isopropoxy-5-(2-thiophen-3-yl-ethoxy)-benzamide is isolated after column chromatography (heptan /ethylacetate) as yellow oil in a yield of 45%; HPLC (method B): 3.63 min; LC-MS (method B): 2.74 min, 462.2 (MH+); 1H-NMR (DMSO-d5, 500 MHz): δ [ppm] 10.78 (s, 1), 7.79 (d, 1H, J=2.2 Hz), 7.468 (dd, 1H, J=3 Hz, J=4.9 Hz), 7.359-7.269 (m, 4H), 7.245-7228 (m, 2H), 7.174-7.139 (m, 2H), 7.11 (dd, 1H, J=1.1 Hz, J=4.9 Hz), 6.648 (d, 1H, J=2.2 Hz), 5.256 (s, 2H), 4.678 (sep, 1H, J=6 Hz), 4.223 (t, 2H, J=6.9 Hz), 3.049 (t, 2H, J=6.9 Hz), 1.262 (d, 6H, J=6 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08236824B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-9da74deedd434072b2758162eaa0882b
출처 메모uspto-grants-2012_08