【结 构 式】 |
【药物名称】OSI-461, CP-461 【化学名称】N-Benzyl-2-[5-fluoro-2-methyl-1-[(Z)-(pyridin-4-yl)methylene]-1H-inden-3-yl]acetamide hydrochloride 【CA登记号】227619-96-7, 227619-92-3 (free base) 【 分 子 式 】C25H22ClFN2O 【 分 子 量 】420.91829 |
【开发单位】OSI (Originator) 【药理作用】Antineoplastic Enhancing Agents, GASTROINTESTINAL DRUGS, Inflammatory Bowel Disease, Agents for, Leukemia Therapy, Lymphocytic Leukemia Therapy, Modulators of the Therapeutic Activity of Antineoplastic Agents, ONCOLYTIC DRUGS, Prostate Cancer Therapy, Renal Cancer Therapy, Solid Tumors Therapy, Apoptosis Inducers, Phosphodiesterase II (PDE2A) Inhibitors, Phosphodiesterase V (PDE5A) Inhibitors |
合成路线1
Heating p-fluorobenzaldehyde (I) with propionic anhydride (II) in the presence of sodium propionate affords methyl cinnamic acid derivative (III), which is then hydrogenated over Pd/C in EtOH to provide methyl hydrocinnamic acid derivative (IV). Ring closure of (IV) is then performed by heating with polyphosphoric acid to yield methylindanone derivative (V). Condensation of (V) with cyanoacetic acid (VI) by means of ammonium acetate and HOAc in refluxing toluene followed by treatment with KOH in refluxing EtOH provides acetic acid derivative (VII), which is then converted into acetyl chloride compound (VIII) by reaction with oxalyl chloride in refluxing THF. Coupling of (VIII) with benzylamine (IX) in refluxing CH2Cl2 gives indenylacetamide derivative (X), which is finally condensed with 4-pyridinecarboxaldehyde (XI) by means of NaOMe in MeOH to furnish the desired compound.
【1】 Piazza, G.; Gross, P.; Brendel, K.; Sperl, G.; Pamukcu, R. (Cell Pathways, Inc.; University of Arizona); N-Benzyl-3-indenylacetamides derivs. for treating neoplasia. EP 1044187; US 5948779; US 6066634; WO 9931065 . |
【2】 Mayle, M.J.; Menander, K.B. (Cell Pathways, Inc.); A method for treating patients with acne by administering a cyclic GMP PDE inhibitor. WO 0044372 . |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(I) | 12337 | 4-fluorobenzaldehyde | 459-57-4 | C7H5FO | 详情 | 详情 |
(II) | 20095 | propionic anhydride | 123-62-6 | C6H10O3 | 详情 | 详情 |
(III) | 48870 | (Z)-3-(4-fluorophenyl)-2-methyl-2-propenoic acid | C10H9FO2 | 详情 | 详情 | |
(IV) | 48871 | 3-(4-fluorophenyl)-2-methylpropionic acid | C10H11FO2 | 详情 | 详情 | |
(V) | 48872 | 6-Fluoro-2-methylindanone | C10H9FO | 详情 | 详情 | |
(VI) | 48873 | 2-Oxopropionitrile; Acetylcyanide; Pyruvonitrile | C3H3NO | 详情 | 详情 | |
(VII) | 48874 | 2-(5-fluoro-2-methyl-1H-inden-3-yl)acetic acid | C12H11FO2 | 详情 | 详情 | |
(VIII) | 48878 | 2-(5-fluoro-2-methyl-1H-inden-3-yl)acetyl chloride | C12H10ClFO | 详情 | 详情 | |
(IX) | 15147 | Benzylamine; Phenylmethanamine | 100-46-9 | C7H9N | 详情 | 详情 |
(X) | 48877 | N-benzyl-2-(5-fluoro-2-methyl-1H-inden-3-yl)acetamide | C19H18FNO | 详情 | 详情 | |
(XI) | 17203 | 4-Pyridinecarboxaldehyde; isonicotinaldehyde | 872-85-5 | C6H5NO | 详情 | 详情 |