{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Base Information

Chemical Name:{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester
CAS No.:105763-67-5
Molecular Formula:C₂₂H₃₃N₃O₆
Molecular Weight:435.521
Hs Code.:

Synonyms:{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

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Chemical Property of {5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of {5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

There total 6 articles about {5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester 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:

: 100-60-7
N-methylcyclohexylamine

: 105763-67-5
{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

2: NaBH₃CN / ethanol / 3 h

With sodium cyanoborohydride; sodium carbonate; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00385a011

Reference yield:

: 42454-06-8
2-nitro-5-hydroxybenzaldehyde

: 105763-67-5
{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / K₂CO₃ / dimethylformamide / 1 h / 100 °C

2: 96 percent / aq. KOH / ethanol

3: oxalyl chloride / benzene; dimethylformamide / 1 h / Ambient temperature

4: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

5: NaBH₃CN / ethanol / 3 h

With potassium hydroxide; oxalyl dichloride; sodium cyanoborohydride; sodium carbonate; potassium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a011

Reference yield:

: 94193-35-8
ethyl 4-((3-formyl-4-nitrophenyl)oxy)butyrate

: 105763-67-5
{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / aq. KOH / ethanol

2: oxalyl chloride / benzene; dimethylformamide / 1 h / Ambient temperature

3: aq. Na₂CO₃ / tetrahydrofuran / 1 h / Ambient temperature

4: NaBH₃CN / ethanol / 3 h

With potassium hydroxide; oxalyl dichloride; sodium cyanoborohydride; sodium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a011