6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

Base Information

Chemical Name:6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide
CAS No.:543745-09-1
Molecular Formula:C₂₆H₂₇N₅O₄
Molecular Weight:473.531
Hs Code.:

Synonyms:6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

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Chemical Property of 6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

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Technology Process of 6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

There total 12 articles about 6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide 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: 78.0%

: 543745-08-0
1-(4-methoxyphenyl)-7-oxo-6-(4-piperidinyl)-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

: 446-52-6
2-Fluorobenzaldehyde

: 543745-09-1
6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

Guidance literature:: With potassium carbonate; In dimethyl sulfoxide; at 85 ℃; for 16h;
DOI:10.1016/j.bmcl.2006.11.071

Reference yield: 78.0%

: 543745-09-1
6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

Guidance literature:

Reference yield:

: N-(1-benzylpiperidin-4-yl)-5-bromopentanamide

: 543745-09-1
6-[1-(2-formylphenyl)-4-piperidinyl]-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 9 steps

1: t-BuOK / tetrahydrofuran / 0.5 h / 0 °C

2: 85 percent / PCl₅ / CHCl₃ / 3 h / Heating

3: 86 percent / Heating

4: Et₃N / toluene / 85 °C

5: aq. HCl / CH₂Cl₂ / 4 h / 20 °C

6: 94 percent / H₂; HOAc / Pd/C / methanol / 3 h / 20 °C

7: 50 percent / Et₃N; copper(II) acetate / 72 h / 20 °C

8: ammonia / ethane-1,2-diol / 2 h / 85 °C

9: 78 percent / K₂CO₃ / dimethylsulfoxide / 16 h / 85 °C

With hydrogenchloride; phosphorus pentachloride; potassium tert-butylate; ammonia; hydrogen; copper diacetate; potassium carbonate; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; ethylene glycol; dimethyl sulfoxide; toluene;
DOI:10.1016/j.bmcl.2006.11.071