tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate
CAS No.:1433958-18-9
Molecular Formula:C₂₈H₃₉N₅O₄
Molecular Weight:509.649
Hs Code.:

Synonyms:tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

There total 4 articles about tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)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:

: 1433958-17-8
tert-butyl 4-(((2-cyano-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

: 1433958-18-9
tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

Guidance literature:: With dihydrogen peroxide; sodium hydroxide; In ethanol; water; dimethyl sulfoxide; at 50 ℃;

Reference yield:

: 908111-29-5
2-bromo-4-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)benzonitrile

: 1433958-18-9
tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium tert-butylate / toluene / 6 h / Inert atmosphere; Reflux

2: dihydrogen peroxide; sodium hydroxide / ethanol; water; dimethyl sulfoxide / 50 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium tert-butylate; dihydrogen peroxide; sodium hydroxide; In ethanol; water; dimethyl sulfoxide; toluene;

Reference yield:

: 36282-26-5
2-bromo-4-fluorobenzonitrile

: 1433958-18-9
tert-butyl 4-(((2-carbamoyl-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indazol-1-yl)phenyl)amino)methyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / dimethyl sulfoxide

1.2: 45 °C

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium tert-butylate / toluene / 6 h / Inert atmosphere; Reflux

3.1: dihydrogen peroxide; sodium hydroxide / ethanol; water; dimethyl sulfoxide / 50 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium tert-butylate; dihydrogen peroxide; sodium hydride; sodium hydroxide; In ethanol; water; dimethyl sulfoxide; toluene;