反应 #2320155

ord-64a7e22ef0964347af69f3d7424b8a93

反应方程式

Cc1ccccc1CC(N)=O
2-o-tolylacetamide
Cl.NNc1cccc(C(F)(F)F)c1Cl
2-chloro-3-trifluoromethylphenylhydrazine hydrochloride
Cl.NNc1ccccc1
phenylhydrazine hydrochloride
O=CNC(=O)Cc1ccccc1
N-formylphenylacetamide
NC(=O)C1CCc2ccccc21
indan-1-carboxamide
FC(F)(F)c1cccc(-n2ncnc2C2CCc3ccccc32)c1Cl
title compound
FC(F)(F)c1cccc(-n2ncnc2C2CCc3ccccc32)c1Cl
1-[2-chloro-3-(trifluoromethyl)phenyl]-5-(2,3-dihydro-1H-inden-1-yl)-1H-1,2,4-triazole

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The title compound was prepared
  2. 2
    其他prepared
  3. 3
    其他The residue was purified by flash chromatography (40% ethyl acetate/hexanes)

实验过程

The title compound was prepared using the procedure as described in Example 80 substituting 2-chloro-3-trifluoromethylphenylhydrazine hydrochloride for phenylhydrazine hydrochloride and substituting N-formyl-2,3-dihydro-1H-indene-1-carboxamide (prepared using the procedure as described in Example 76A, substituting from indan-1-carboxamide [Seidl Tetrahedron 1964, 20, 633] for 2-o-tolylacetamide) for N-formylphenylacetamide. The residue was purified by flash chromatography (40% ethyl acetate/hexanes) to provide the title compound. MS (ESI) m/e: 364 (M+H)+; 1H NMR (DMSO-d6) δ 2.05-2.45 (m, 2H), 2.8-3.05 (m, 2H), 4.29-4.35 (t, 1H), 6.95-7.05 (bs, 1H), 7.03-7.1 (t, 1H), 7.1-7.21 (t, 1H), 7.2-7.3 (d, 1H), 7.78-7.82 (t, 2H), 8.0-8.01 (bs, 0.5H), 8.18 (s, 1H), 8.22 (bs, 0.5H); Anal. calcd. for C, 59.43; H, 3.60; N, 11.55. Found C, 59.20; H, 3.34; N, 11.48

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07709469B2uspto-grants-2010_05