cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

Base Information

Chemical Name:cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester
CAS No.:948304-27-6
Molecular Formula:C₂₆H₃₆N₂O₄
Molecular Weight:440.583
Hs Code.:

Synonyms:cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

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Chemical Property of cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

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Technology Process of cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

There total 4 articles about cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic 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:

: 948304-34-5
C₁₅H₂₁NO₃

: 4411-25-0
1-adamantyl isocyanate

: 948304-27-6
cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm070270t

Reference yield:

: 948304-23-2
cis-4-[4-(1,3-dioxo-1,3-dihydroisoindol-2-yl)cyclohexyloxy]benzoic acid ethyl ester

: 948304-27-6
cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / CH₂Cl₂; methanol / 24 h / 20 °C

2: Et₃N / dimethylformamide / 0 - 20 °C

With hydrazine hydrate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm070270t

Reference yield:

: 50910-54-8
trans-4-aminocyclohexanol hydrochloride

: 948304-27-6
cis-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy]benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: K₂CO₃ / H₂O / 0.5 h / 20 °C

2: 78 percent / triphenylphosphine; diisopropyl azodicarboxylate / tetrahydrofuran / 20 °C

3: hydrazine hydrate / CH₂Cl₂; methanol / 24 h / 20 °C

4: Et₃N / dimethylformamide / 0 - 20 °C

With di-isopropyl azodicarboxylate; potassium carbonate; hydrazine hydrate; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 2: Mitsunobu coupling;
DOI:10.1021/jm070270t