benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

Base Information

Chemical Name:benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate
CAS No.:816464-48-9
Molecular Formula:C₂₇H₂₅N₃O₄S
Molecular Weight:487.579
Hs Code.:

Synonyms:benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

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Chemical Property of benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

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Technology Process of benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

There total 5 articles about benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-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:

Reference yield:

: sodium 3-cyano-6-oxo-1-phenyl-1,6-dihydro-pyridine-2-thiolate

: 816464-47-8
benzyl 4-(2-bromoacetyl)piperidine-1-carboxylate

: 816464-48-9
benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In acetonitrile; at 50 ℃; for 8h;

Reference yield:

: 10314-98-4
1-benzyloxycarbonylpiperidine-4-carboxylic acid

: 816464-48-9
benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 2.5 h / 20 °C

2: methyl magnesium ⁽¹⁺⁾; bromide / tetrahydrofuran / 1 h / 0 - 20 °C

3: bromine / methanol / 2 h / 0 - 20 °C

4: potassium carbonate / acetonitrile / 8 h / 50 °C

With dmap; bromine; methyl magnesium ⁽¹⁺⁾; bromide; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; methanol; dichloromethane; acetonitrile;

Reference yield:

: 160809-34-7
4-acetyl-piperidine-1-carboxylic acid benzyl ester

: 816464-48-9
benzyl 4-[(3-amino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridin-2-yl)carbonyl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: bromine / methanol / 2 h / 0 - 20 °C

2: potassium carbonate / acetonitrile / 8 h / 50 °C

With bromine; potassium carbonate; In methanol; acetonitrile;