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methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate

Base Information Edit
  • Chemical Name:methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate
  • CAS No.:334792-25-5
  • Molecular Formula:C17H19FN4O2
  • Molecular Weight:330.362
  • Hs Code.:
  • Mol file:334792-25-5.mol
methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate

Synonyms:methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate

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Chemical Property of methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate Edit
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Technology Process of methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate

There total 7 articles about methyl 4-fluoro-3-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 120 ℃; for 6h;
DOI:10.1016/j.bmc.2006.01.062
Guidance literature:
Multi-step reaction with 5 steps
1: 12 percent / cesium carbonate; (R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl / palladium(II) acetate / toluene / 7 h / 90 - 100 °C
2: triethylamine / CH2Cl2 / 0.17 h / 20 °C
3: sodium azide / dimethylformamide / 14 h / 80 °C
4: 288 mg / hydrogen / Pd/C / dioxane; H2O / 10 h / 20 °C
5: 67 percent / ethyldiisopropylamine / dimethylsulfoxide / 6 h / 120 °C
With sodium azide; hydrogen; caesium carbonate; (R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; palladium diacetate; In 1,4-dioxane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmc.2006.01.062
Guidance literature:
Multi-step reaction with 4 steps
1: triethylamine / CH2Cl2 / 0.17 h / 20 °C
2: sodium azide / dimethylformamide / 14 h / 80 °C
3: 288 mg / hydrogen / Pd/C / dioxane; H2O / 10 h / 20 °C
4: 67 percent / ethyldiisopropylamine / dimethylsulfoxide / 6 h / 120 °C
With sodium azide; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In 1,4-dioxane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2006.01.062
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