{(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

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Chemical Name:{(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester
CAS No.:357922-56-6
Molecular Formula:C₂₀H₃₆N₂O₅
Molecular Weight:384.516
Hs Code.:

Synonyms:{(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

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Chemical Property of {(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

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Technology Process of {(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

There total 9 articles about {(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl 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: 99.0%

: 357922-53-3
{(1S,2S)-2-[2-((1S,2S)-2-Azido-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

: 357922-56-6
{(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 2h; under 750.06 Torr;
DOI:10.1002/1521-3773(20010601)40:11<2076::AID-ANIE2076>3.0.CO;2-G

Reference yield:

: 357922-50-0
(1'S,2'S)-(2'-azido-cyclohexyl)oxy-acetic-acid-tert-butylester

: 357922-56-6
{(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: TFA / CH₂Cl₂ / 1.5 h / 20 °C

1.2: DIEA / dimethylformamide / 1 h / 0 °C

2.1: 70 percent / DIEA / dimethylformamide / 6 h / 0 - 20 °C

3.1: H₂ / 5 percent Pd-C / methanol

With hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol048861q

Reference yield:

: 286-20-4
cyclohexene oxide

: 357922-56-6
{(1S,2S)-2-[2-((1S,2S)-2-Amino-cyclohexyloxy)-acetylamino]-cyclohexyloxy}-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: (R,R)-Salen-CrN₃ / diethyl ether; propan-2-ol / 36 h / 4 °C

1.2: TFA / methanol / 1 h / 20 °C

1.3: 95 percent / tetrabutylammonium bromide; aq. NaOH / toluene / 18 h / 20 °C

2.1: TFA / CH₂Cl₂ / 1.5 h / 20 °C

2.2: DIEA / dimethylformamide / 1 h / 0 °C

3.1: 70 percent / DIEA / dimethylformamide / 6 h / 0 - 20 °C

4.1: H₂ / 5 percent Pd-C / methanol

With (R,R)-Salen-CrN₃; hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/ol048861q