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【结 构 式】

【分子编号】66476

【品名】4-(chloromethyl)-N-(4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)benzamide

【CA登记号】404844-11-7

【 分 子 式 】C24H20ClN5O

【 分 子 量 】429.909

【元素组成】C 67.05% H 4.69% Cl 8.25% N 16.29% O 3.72%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

 

1 Kompella A, Bhujanga Rao AKS, Venkaiah Chowdary N, et aL 2004. Process for the preparation of the anti-cancer drug imatinib and its analogs via aminolysis of a (chloromethyl benzamide intermediate. WO 2004108699(本专利申请人为: Natco Pharma Limited, India)
2 Szczepek W, Luniewski W, Kaczmarek L, et aL 2006.A process for preparation of imatinib base. W0 2006071130(本专利申请人为: Instytut Farmaceutyczny, Pol)
3 Szakacs Z,Beni S,VargaZ,et aL 2005. Acid-base profiling of imatinib(gleevec) and its fragments. J Med Chem,8(1): 249一255
4 Zimmermann J.Buchdunger E, Mett H, et aL 1997. Potent and selective inhibitors of the abl-kinase: phenylaminopyrimidine (PAP) derivatives. Bioorg Med Chem Lett,7(2): 187~191
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) 47518 2-Amino-4-nitrotoluene; 5-Nitro-o-toluidine; 4-Nitro-2-aminotoluene; 2-methyl-5-nitrophenylamine; 2-methyl-5-nitroaniline 99-55-8 C7H8N2O2 详情 详情
(II) 47517 N-(2-methyl-5-nitrophenyl)guanidine 152460-07-6 C8H10N4O2 详情 详情
(III) 47516 (E)-3-(dimethylamino)-1-(3-pyridinyl)-2-propen-1-one 123367-26-0 C10H12N2O 详情 详情
(IV) 47519 N-(2-methyl-5-nitrophenyl)-N-[4-(3-pyridinyl)-2-pyrimidinyl]amine; N-(2-methyl-5-nitrophenyl)-4-(3-pyridinyl)-2-pyrimidinamine 152460-09-8 C16H13N5O2 详情 详情
(V) 47520 4-methyl-N(3)-[4-(3-pyridinyl)-2-pyrimidinyl]-1,3-benzenediamine; N-(5-amino-2-methylphenyl)-N-[4-(3-pyridinyl)-2-pyrimidinyl]amine 152460-10-1 C16H15N5 详情 详情
(VI) 49112 4-(Chloromethyl)benzoyl chloride; p-(Chloromethyl)benzoyl chloride 876-08-4 C8H6Cl2O 详情 详情
(VII) 66476 4-(chloromethyl)-N-(4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)benzamide 404844-11-7 C24H20ClN5O 详情 详情
(VIII) 10061 1-Methylpiperazine; 1-Methyl piperazine; N-Methylpiperazine 109-01-3 C5H12N2 详情 详情
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