(1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

Base Information

Chemical Name:(1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate
CAS No.:1357921-74-4
Molecular Formula:C₂₄H₄₂N₂O₃Si
Molecular Weight:434.695
Hs Code.:

Synonyms:(1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

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Chemical Property of (1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

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Technology Process of (1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

There total 5 articles about (1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate 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: 100.0%

: 1357921-73-3
(1s,4s)-methyl 4-((2-nitro-5-(((triisopropylsilyl)oxy)methyl)-phenyl)amino)cyclohexanecarboxylate

: 1357921-74-4
(1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

Guidance literature:: With palladium 10% on activated carbon; ammonium formate; In ethanol; at 20 ℃; Inert atmosphere;
DOI:10.1021/jm3005866

Reference yield:

: 3685-23-2
cis-4-aminocyclohexane-1-carboxylic acid

: 1357921-74-4
(1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid / 18 h / 80 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 h / 50 °C

3: palladium 10% on activated carbon; ammonium formate / ethanol / 20 °C / Inert atmosphere

With sulfuric acid; palladium 10% on activated carbon; ammonium formate; N-ethyl-N,N-diisopropylamine; In ethanol; acetonitrile;
DOI:10.1021/jm3005866

Reference yield:

: 62456-15-9,75143-07-6
methyl (1s,4s)-4-aminocyclohexane-1-carboxylate

: 1357921-74-4
(1s,4s)-methyl 4-(2-amino-5-((triisopropylsilyloxy)methyl)phenylamino)cyclohexanecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 h / 50 °C

2: palladium 10% on activated carbon; ammonium formate / ethanol / 20 °C / Inert atmosphere

With palladium 10% on activated carbon; ammonium formate; N-ethyl-N,N-diisopropylamine; In ethanol; acetonitrile;
DOI:10.1021/jm3005866