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2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester

Base Information Edit
  • Chemical Name:2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester
  • CAS No.:183433-89-8
  • Molecular Formula:C24H29NO5
  • Molecular Weight:411.498
  • Hs Code.:
  • Mol file:183433-89-8.mol
2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester

Synonyms:2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester

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Chemical Property of 2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester Edit
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Technology Process of 2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester

There total 8 articles about 2,3-dihydro-6-methyl-7-[1-(phenylmethoxy)-propyl]-1,5-indolizinedione-2-carboxylic acid 1,1-dimethylethyl ester 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:
Multi-step reaction with 4 steps
1.1: sodium hydride / tetrahydrofuran / 0.5 h / 20 °C
1.2: 90 percent / tetrahydrofuran / 8 h / 20 °C
2.1: 89 percent / potassium acetate; palladium acetate; 1,3-bis(diphenylphosphino)propane / dimethylformamide / 25 h / 85 °C / 775.72 Torr
3.1: 97 percent / sodium iodide; trimethylsilyl chloride / acetonitrile / 24 h / 20 °C
4.1: 85 percent / cesium carbonate / dimethylsulfoxide / 3 h / 65 °C
With chloro-trimethyl-silane; 1,3-bis-(diphenylphosphino)propane; potassium acetate; palladium diacetate; sodium hydride; caesium carbonate; sodium iodide; In tetrahydrofuran; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/jhet.5570400407
Guidance literature:
Multi-step reaction with 7 steps
1.1: n-BuLi / heptane; hexane / 1.75 h / 0 °C
1.2: 66 percent / heptane; hexane / 2 h / 0 °C
2.1: 99 percent / aq. trifluoroacetic acid / 4 h / 40 °C
3.1: 85 percent / sodium borohydride / aq. methanol / 0.33 h / 0 °C
4.1: sodium hydride / tetrahydrofuran / 0.5 h / 20 °C
4.2: 90 percent / tetrahydrofuran / 8 h / 20 °C
5.1: 89 percent / potassium acetate; palladium acetate; 1,3-bis(diphenylphosphino)propane / dimethylformamide / 25 h / 85 °C / 775.72 Torr
6.1: 97 percent / sodium iodide; trimethylsilyl chloride / acetonitrile / 24 h / 20 °C
7.1: 85 percent / cesium carbonate / dimethylsulfoxide / 3 h / 65 °C
With sodium tetrahydroborate; n-butyllithium; chloro-trimethyl-silane; 1,3-bis-(diphenylphosphino)propane; potassium acetate; palladium diacetate; sodium hydride; caesium carbonate; trifluoroacetic acid; sodium iodide; In tetrahydrofuran; methanol; hexane; n-heptane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/jhet.5570400407
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