NSC-D703786, NSC-703786, 5F-DF-203, 5F-203

4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯胺Chemical Name: 4-(5-Fluorobenzothiazol-2-yl)-2-methylphenylamine
CAS No. 260443-89-8
项目整合开发状态: Preclinical
项目研究机构: National Cancer Institute (Originator), University of Nottingham (Originator)
合成路线:The reaction of 5-fluorobenzothiazol-2-amine (I) with KOH in refluxing water gives the disulfide (II),which is treated with 3-methyl-4-nitrobenzoyl chloride (III) in refluxing pyridine to yield the bis-benzamide (IV).Finally,this compound is reductively cyclized by reaction with SnCl2 and HCl in ethanol/water to afford the target aminophenyl benzothiazole.

合成路线:Synthesis of intermediate (VII): Conversion of 3-fluoroaniline (I) into 2-amino-5-fluorobenzothiazole (III) can be achieved by first coupling with isocyanate (II) followed by hydrolysis with NaOH,reaction with Br2 and finally heating treatment.Dimerization of substituted benzothiazole (III) by means of refluxing aqueous KOH yields disulfide derivative (IV),which is then condensed with substituted benzoyl chloride (V) in refluxing pyridine to afford derivative (VI).Finally,(VI) is converted into intermediate (VII) by treatment with SnCl2 dihydrate in refluxing HCl/EtOH.Alternatively,intermediate (VII) can be synthesized as follows: substituted aniline (VIII) is first brominated via a Sandmeyer reaction with NaNO2 in HBr and CuBr,and then the nitro group is reduced with SnCl2 in refluxing EtOH to provide derivative (IX).Condensation of (IX) with substituted benzoyl chloride (V) in refluxing pyridine yields amide (X),which is then first treated with Lawesson's reagent and HMPA and then with NaH in NMP to afford benzothiazole derivative (XI).Finally,the nitro group of (XI) is reduced with SnCl2 in refluxing EtOH to yield intermediate (VII).Synthesis of EN 295753: The desired compound can finally be obtained by coupling of intermediate (VII) with Boc-Lys(Boc)-OH (XII) by means of carbodiimide WSC.HCl and HOBt in CH2Cl2,followed by Boc removal with HCl (gas) in CH2Cl2.