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Methyl 6-pivaloyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-2-carboxylate

Base Information Edit
  • Chemical Name:Methyl 6-pivaloyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-2-carboxylate
  • CAS No.:1259287-87-0
  • Molecular Formula:C14H19NO3S
  • Molecular Weight:281.376
  • Hs Code.:
  • Mol file:1259287-87-0.mol
Methyl 6-pivaloyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-2-carboxylate

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Chemical Property of Methyl 6-pivaloyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-2-carboxylate Edit
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Technology Process of Methyl 6-pivaloyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-2-carboxylate

There total 5 articles about Methyl 6-pivaloyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-2-carboxylate 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 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; at 20 - 36 ℃;
Guidance literature:
Multi-step reaction with 5 steps
1.1: potassium carbonate / N,N-dimethyl-formamide / 48.5 h / 0 - 20 °C
2.1: acetonitrile / 6 h / 40 °C
3.1: hydrogen; platinum(IV) oxide / methanol
4.1: carbonochloridic acid 1-chloro-ethyl ester; N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 3 h / 0 - 20 °C
4.2: 3 h / Reflux
5.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / dichloromethane / 0.5 h / 20 °C
5.2: 17 h / 20 - 36 °C
With platinum(IV) oxide; carbonochloridic acid 1-chloro-ethyl ester; hydrogen; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm400385r
Guidance literature:
Multi-step reaction with 4 steps
1.1: acetonitrile / 6 h / 40 °C
2.1: hydrogen; platinum(IV) oxide / methanol
3.1: carbonochloridic acid 1-chloro-ethyl ester; N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 3 h / 0 - 20 °C
3.2: 3 h / Reflux
4.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / dichloromethane / 0.5 h / 20 °C
4.2: 17 h / 20 - 36 °C
With platinum(IV) oxide; carbonochloridic acid 1-chloro-ethyl ester; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; methanol; dichloromethane; acetonitrile;
DOI:10.1021/jm400385r
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