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【结 构 式】

【分子编号】33671

【品名】[1-(1,3-benzodioxol-5-ylmethyl)-1H-imidazol-5-yl]methanol

【CA登记号】

【 分 子 式 】C12H12N2O3

【 分 子 量 】232.23896

【元素组成】C 62.06% H 5.21% N 12.06% O 20.67%

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:(IV)

The condensation of piperonylamine (I) with dihydroxyacetone dimer (II) in the presence of potassium thiocyanate produced the mercaptoimidazole (III), which was desulfurized upon treatment with nitric acid and sodium nitrite. The resulting (hydroxymethyl)imidazole (IV) was then converted to the corresponding chloride (V) employing thionyl chloride in chloroform.

1 Lee, J.; Lee, H.; Shin, Y.; et al.; Synthesis and structure-activity relationships of 1-(1(3)H-imidazole-5(4)-yl)-methylpyrroles as farnesyl protein transferase inhibitors (FTPI). 218th ACS Natl Meet (Aug 22 1999, New Orleans) 1999, Abst MEDI 210.
2 Lee, J.H.; Yoo, J.K.; Koh, J.S.; Choi, T.S.; Shin, Y.S.; Kim, K.H.; Jung, W.H.; Kim, J.H.; Lee, S.H.; Ahn, I.A.; Ro, S.G.; Lee, H.I.; Kim, H.S.; Chung, H.H.; Jeong, S.W.; Kwak, T.H. (LG Chem Ltd.); Imidazole derivs. having an inhibitory activity for farnesyl transferase and process for preparation thereof. WO 9928315 .
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) 33669 1,3-benzodioxol-5-ylmethylamine; 1,3-benzodioxol-5-ylmethanamine; 3,4-Methylendioxybenzylamine 2620-50-0 C8H9NO2 详情 详情
(II) 20067 2,5-bis(hydroxymethyl)-1,4-dioxane-2,5-diol 89727-88-8 C6H12O6 详情 详情
(III) 33670 [1-(1,3-benzodioxol-5-ylmethyl)-2-sulfanyl-1H-imidazol-5-yl]methanol C12H12N2O3S 详情 详情
(IV) 33671 [1-(1,3-benzodioxol-5-ylmethyl)-1H-imidazol-5-yl]methanol C12H12N2O3 详情 详情
(V) 33672 1-(1,3-benzodioxol-5-ylmethyl)-5-(chloromethyl)-1H-imidazole C12H11ClN2O2 详情 详情
Extended Information