tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate
CAS No.:1308889-37-3
Molecular Formula:C₃₅H₃₈N₂O₉
Molecular Weight:630.695
Hs Code.:

Synonyms:tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

There total 7 articles about tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)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: 85.0%

: 1160952-27-1
N-(7-hydroxy-8-methoxy-2-oxo-2H-chromen-3-yl)-3',6-dimethoxy-[1,1'-biphenyl]-3-carboxamide

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1308889-37-3
tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1021/jm200148p

Reference yield:

: 1083312-86-0
benzyl 7-hydroxy-8-methoxy-2-oxo-2H-chromen-3-ylcarbamate

: 1308889-37-3
tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / 12 h

2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 12 h

3: triethylamine / tetrahydrofuran / 12 h

4: triethylamine / methanol / 12 h / 20 °C

5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 0 °C

With di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine; In tetrahydrofuran; pyridine; methanol; 5: Mitsunobu reaction;
DOI:10.1021/jm200148p

Reference yield:

: 1083313-05-6
3′,6-dimethoxy-[1,1′-biphenyl]-3-carboxylic acid

: 1308889-37-3
tert-butyl 4-(3-(3',6-dimethoxybiphenyl-3-ylcarboxamido)-8-methoxy-2-oxo-2H-chromen-7-yloxy)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / tetrahydrofuran

2: triethylamine / tetrahydrofuran / 12 h

3: triethylamine / methanol / 12 h / 20 °C

4: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 0 °C

With thionyl chloride; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; 4: Mitsunobu reaction;
DOI:10.1021/jm200148p