• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】35786

【品名】ethyl 1-(2,4-dichlorophenyl)-4-methyl-5-(2-nitrophenyl)-1H-pyrazole-3-carboxylate

【CA登记号】

【 分 子 式 】C19H15Cl2N3O4

【 分 子 量 】420.25132

【元素组成】C 54.3% H 3.6% Cl 16.87% N 10% O 15.23%

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:(XIIa)

Propiophenone (IX) was condensed with diethyl oxalate to give diketone (X). Reaction with hydrazine (III) afforded pyrazole (XI). Nitration of (XI) by nitronium tetrafluoborate in acetonitrile gave a mixture of para- and ortho-nitrated compounds (XIIa-b), which were used without separation. Ester hydrolysis, followed by chlorination to (XIIIa-b) and condensation with 1-aminopiperidine (VI) gave the corresponding mixture of para- and ortho-nitro amides, which were separated by flash chromatography. The required para-isomer (XIV) was reduced by hydrazine and Raney Nickel to aniline (XV). This was finally converted to the title iodide via the reaction of the diazonium salt with NaI.

1 Fan, P.; Liu, Q.; Lan, R.; et al.; Structure-activity relationships of pyrazole derivatives as cannabinoid receptor antagonists. J Med Chem 1999, 42, 4, 769.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XIIa) 35786 ethyl 1-(2,4-dichlorophenyl)-4-methyl-5-(2-nitrophenyl)-1H-pyrazole-3-carboxylate C19H15Cl2N3O4 详情 详情
(XIIb) 35787 ethyl 1-(2,4-dichlorophenyl)-4-methyl-5-(4-nitrophenyl)-1H-pyrazole-3-carboxylate C19H15Cl2N3O4 详情 详情
(XIIIa) 35788 1-(2,4-dichlorophenyl)-4-methyl-5-(2-nitrophenyl)-1H-pyrazole-3-carbonyl chloride C17H10Cl3N3O3 详情 详情
(XIIIb) 35789 1-(2,4-dichlorophenyl)-4-methyl-5-(4-nitrophenyl)-1H-pyrazole-3-carbonyl chloride C17H10Cl3N3O3 详情 详情
(III) 35778 1-(2,4-dichlorophenyl)hydrazine 5446-18-4 C6H6Cl2N2 详情 详情
(VI) 35781 1-piperidinylamine; 1-piperidinamine 2213-43-6 C5H12N2 详情 详情
(IX) 33531 propiophenone 93-55-0 C9H10O 详情 详情
(X) 35784   C13H13LiO4 详情 详情
(XI) 35785 ethyl 1-(2,4-dichlorophenyl)-4-methyl-5-phenyl-1H-pyrazole-3-carboxylate C19H16Cl2N2O2 详情 详情
(XIV) 35790 1-(2,4-dichlorophenyl)-4-methyl-5-(4-nitrophenyl)-N-(1-piperidinyl)-1H-pyrazole-3-carboxamide C22H21Cl2N5O3 详情 详情
(XV) 35791 5-(4-aminophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-(1-piperidinyl)-1H-pyrazole-3-carboxamide C22H23Cl2N5O 详情 详情
Extended Information