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HRID 251334生成日期:2026年10月23日

3-肼基-4-甲基苯甲酸盐酸盐 → 3-[5-Amino-4-(3-iodobenzoyl)-pyrazol-1-yl]-4-methylbenzoic acid

https://huagongshe.com/zh-CN/reaction/251334

反应方程式

参与物

角色名称HCID投料
反应物3-肼基-4-甲基苯甲酸盐酸盐HCID 56777508—
反应物2-(3-Iodobenzoyl)-3-phenylaminoacrylonitrileHCID 67024274—
溶剂乙醇HCID 702—
溶剂(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮HCID 887—
产物3-[5-Amino-4-(3-iodobenzoyl)-pyrazol-1-yl]-4-methylbenzoic acidHCID 1115507222%

反应条件

温度75 °C

反应步骤

To a stirred solution of 3-hydrazino-4-methyl-benzoic acid hydrochloride 1 (Example 3A, 314 mg, 1.54 mmol, 1.0 eq) in 50 mL of ethanol and 5 mL of methanol was added 2-(3-iodo-benzoyl)-3-phenylamino-acrylonitrile 2 (579 mg, 1.54 mmol, preparation: International Patent Application Publication No. WO 02/57101 A1, pg. 84). The mixture was heated to 75° C. for 18 h. The precipitated solids were collected on a fritted filter and were washed with ethanol to provide 3-[5-Amino-4-(3-iodo-benzoyl)-pyrazol-1-yl]-4-methyl-benzoic acid 3 (153 mg, 22%) as a white solid. MS m/z 448 [M+H]+; 1H NMR (300 MHz, DMSO-d6)<2.18 (s, 3H), 7.05 (bs, 2H), 7.34 (dd, J1=J2=7.7 Hz), 7.58 (d, J=8.1 Hz, 1H), 7.78 (s, 1H), 7.81 (m, 2H), 7.94 (m, 1H), 7.98 (m, 1H), 8.03 (m, 1H) ppm.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07863314B2
来源数据集uspto-grants-2011_01
ORD IDord-6802a9aa694444c7a5eedb567fdd6746
来源说明uspto-grants-2011_01