1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

Base Information

Chemical Name:1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester
CAS No.:467443-24-9
Molecular Formula:C₂₃H₂₈N₂O₄
Molecular Weight:396.486
Hs Code.:

Synonyms:1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

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Chemical Property of 1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

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Technology Process of 1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

There total 5 articles about 1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl 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:

: 104-01-8
4-Methoxyphenylacetic acid

: 467443-24-9
1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride

2: sodium azide / toluene / 1 h / Heating

3: 83 percent / CHCl₃ / 3 h / 20 °C

With thionyl chloride; sodium azide; In chloroform; toluene;
DOI:10.3797/scipharm.aut-01-204

Reference yield:

: 2746-25-0
p-Methoxybenzyl bromide

: 467443-24-9
1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: AcOH; aq. NaOH

2: thionyl chloride

3: sodium azide / toluene / 1 h / Heating

4: 83 percent / CHCl₃ / 3 h / 20 °C

With sodium hydroxide; thionyl chloride; sodium azide; acetic acid; In chloroform; toluene;
DOI:10.3797/scipharm.aut-01-204

Reference yield:

: 104-47-2
p-methoxybenzylnitrile

: 467443-24-9
1-[3-(4-methoxy-benzyl)-ureido]-cyclohexanecarboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: AcOH; aq. NaOH

2: thionyl chloride

3: sodium azide / toluene / 1 h / Heating

4: 83 percent / CHCl₃ / 3 h / 20 °C

With sodium hydroxide; thionyl chloride; sodium azide; acetic acid; In chloroform; toluene;
DOI:10.3797/scipharm.aut-01-204