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17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid

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  • Chemical Name:17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid
  • CAS No.:1044560-35-1
  • Molecular Formula:C29H34N4O6
  • Molecular Weight:534.612
  • Hs Code.:
17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid

Synonyms:17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid

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Chemical Property of 17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid
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Technology Process of 17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid

There total 4 articles about 17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid 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:
17-(2-methoxy-6-phenyl-pyrimidin-4-yloxy)-13-methyl-2,14-dioxo-3,13-diaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid ethyl ester; With methanol; lithium hydroxide; water; In tetrahydrofuran; at 20 ℃; for 96h;
With citric acid; In tetrahydrofuran; methanol; water;
Guidance literature:
Multi-step reaction with 4 steps
1: triethylsilane; trifluoroacetic acid / dichloromethane / 1 h / 20 °C
2: N-ethyl-N,N-diisopropylamine; HATU / 2.33 h / 0 - 20 °C
3: dichloro(tricyclohexylphosphino)(benzylidene)(1,3-dimesityl-4,5-dihydroimidazol-2-ylidene)ruthenium(III) / 1,2-dichloro-ethane / Heating / reflux
4: methanol; lithium hydroxide; water / tetrahydrofuran / 96 h / 20 °C
With methanol; triethylsilane; lithium hydroxide; water; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; dichloro(tricyclohexylphosphino)(benzylidene)(1,3-dimesityl-4,5-dihydroimidazol-2-ylidene)ruthenium(III); In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane;
Guidance literature:
Multi-step reaction with 2 steps
1: dichloro(tricyclohexylphosphino)(benzylidene)(1,3-dimesityl-4,5-dihydroimidazol-2-ylidene)ruthenium(III) / 1,2-dichloro-ethane / Heating / reflux
2: methanol; lithium hydroxide; water / tetrahydrofuran / 96 h / 20 °C
With methanol; lithium hydroxide; water; dichloro(tricyclohexylphosphino)(benzylidene)(1,3-dimesityl-4,5-dihydroimidazol-2-ylidene)ruthenium(III); In tetrahydrofuran; 1,2-dichloro-ethane;
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