benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

Base Information

Chemical Name:benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate
CAS No.:1146733-36-9
Molecular Formula:C₂₄H₂₉N₃O₄
Molecular Weight:423.512
Hs Code.:

Synonyms:benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

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Chemical Property of benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

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Technology Process of benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

There total 4 articles about benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-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: 81.0%

: 1146733-35-8
benzyl 4-[2-(2-amino-5-methoxy-phenyl)-ethylamino]-2-methyl-piperidine-1-carboxylate

: 530-62-1
1,1'-carbonyldiimidazole

: 1146733-36-9
benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

Guidance literature:: In N,N-dimethyl-formamide; at 20 ℃; for 18h; Reflux;

Reference yield:

: 180149-25-1
2-(5-methoxy-2-nitrophenyl)-ethylamine

: 1146733-36-9
benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 3 h / 0 - 20 °C

2: hydrazine hydrate / palladium 10% on activated carbon / ethanol / 16 h / 20 °C

3: N,N-dimethyl-formamide / 18 h / 20 °C / Reflux

With sodium tris(acetoxy)borohydride; hydrazine hydrate; acetic acid; palladium 10% on activated carbon; In ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 89302-15-8
2-(5-methoxy-2-nitrophenyl)acetonitrile

: 1146733-36-9
benzyl 4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-2-methyl-piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: borane-THF / tetrahydrofuran; methanol / 10 - 20 °C / Reflux; Inert atmosphere

2: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 3 h / 0 - 20 °C

3: hydrazine hydrate / palladium 10% on activated carbon / ethanol / 16 h / 20 °C

4: N,N-dimethyl-formamide / 18 h / 20 °C / Reflux

With borane-THF; sodium tris(acetoxy)borohydride; hydrazine hydrate; acetic acid; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;