5-[2-(tert-butoxycarbonylamino)ethyl]-1-phenyl-1H-pyrazole-4-[N-(3-dimethylamino-1-prop-1-yl)carboxamide] | 1188338-79-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 5-[2-(tert-butoxycarbonylamino)ethyl]-1-phenyl-1H-pyrazole-4-[N-(3-dimethylamino-1-prop-1-yl)carboxamide]
• CAS: 1188338-79-5
• 化学式: C₂₂H₃₃N₅O₃
• 分子量: 415.536
• InChiKey: JVIFSFIFYKYVKF-UHFFFAOYSA-N

反应信息

• 作为反应物：
  描述：

  5-[2-(tert-butoxycarbonylamino)ethyl]-1-phenyl-1H-pyrazole-4-[N-(3-dimethylamino-1-prop-1-yl)carboxamide] 在 盐酸 作用下， 以 乙酸乙酯 为溶剂， 反应 2.5h， 以85%的产率得到5-(2-aminoethyl)-1-phenyl-1H-pyrazole-4-{N-[3-(dimethylamino)prop-1-yl]carboxamide} dihydrochloride
  参考文献：
  名称：

  A synthesis of 1-substituted 5-[2-(acylamino)ethyl]-1H-pyrazole-4-carboxamides

  摘要：

  A seven-step synthesis of 1-substituted 5-(2-acylaminoethyl)-1H-pyi-azole-4-carboxamides 20 as the pyrazole analogues of histamine was developed. The synthesis starts with a three-step preparation of N(1)-substituted methyl 5-(2-tert-butoxycarbonylaminoethyl)-1H-pyrazole-4-carboxylates 7 from commercially available Boc-beta-alanine (1). Subsequent four-step transformation of the key-intermediates 7 into the final products 20 was performed following two complementary reaction sequences comprising acidolytic removal of the Boc group, hydrolysis of the COOMe group, amidations of the COOH group, and acylations of the NH2 group. The Structures of pyrazole derivatives were determined by spectroscopic methods and by X-ray diffraction. (C) 2009 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2009.06.021
• 作为产物：
  描述：

  、 N,N-二甲基-1,3-二氨基丙烷 在 三乙胺 作用下， 以 乙腈 为溶剂， 反应 5.0h， 以82 mg的产率得到5-[2-(tert-butoxycarbonylamino)ethyl]-1-phenyl-1H-pyrazole-4-[N-(3-dimethylamino-1-prop-1-yl)carboxamide]
  参考文献：
  名称：

  A synthesis of 1-substituted 5-[2-(acylamino)ethyl]-1H-pyrazole-4-carboxamides

  摘要：

  A seven-step synthesis of 1-substituted 5-(2-acylaminoethyl)-1H-pyi-azole-4-carboxamides 20 as the pyrazole analogues of histamine was developed. The synthesis starts with a three-step preparation of N(1)-substituted methyl 5-(2-tert-butoxycarbonylaminoethyl)-1H-pyrazole-4-carboxylates 7 from commercially available Boc-beta-alanine (1). Subsequent four-step transformation of the key-intermediates 7 into the final products 20 was performed following two complementary reaction sequences comprising acidolytic removal of the Boc group, hydrolysis of the COOMe group, amidations of the COOH group, and acylations of the NH2 group. The Structures of pyrazole derivatives were determined by spectroscopic methods and by X-ray diffraction. (C) 2009 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2009.06.021