methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

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Chemical Name:methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate
CAS No.:1423134-76-2
Molecular Formula:C₃₁H₄₁N₃O₅
Molecular Weight:535.684
Hs Code.:

Synonyms:methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

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Chemical Property of methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

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Technology Process of methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

There total 6 articles about methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate 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:

: 1423134-75-1
(3S)-3-[3-(benzyloxy)phenyl]-2-(methoxycarbonyl)-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoic acid

: 1423134-76-2
methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

Guidance literature:: With triethylamine; In tetrahydrofuran; at 60 ℃; for 4h;

Reference yield:

: 1700-37-4
3-Benzyloxybenzaldehyde

: 1423134-76-2
methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

Guidance literature:: Multi-step reaction with 6 steps

1: formic acid / tetrahydrofuran; water / 96 h

2: caesium carbonate; 1-{3,5-bis(trifluoromethyl)phenyl}-3-{(1R,2R)-2-(dimethylamino)cyclohexyl}thiourea / water; toluene / 144 h / -20 - 0 °C

3: formic acid / 20 h / 0 - 5 °C

4: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 0 °C

5: formic acid / 120 h / 20 °C

6: triethylamine / tetrahydrofuran / 4 h / 60 °C

With formic acid; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; 1-{3,5-bis(trifluoromethyl)phenyl}-3-{(1R,2R)-2-(dimethylamino)cyclohexyl}thiourea; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1423134-70-6
tert-butyl {[3-(benzyloxy)phenyl](phenylsulfonyl)methyl}carbamate

: 1423134-76-2
methyl (3S)-3-[3-(benzyloxy)phenyl]-3-[({(3R)-1-[3-(piperidin-4-yl)propanoyl]piperidin-3-yl}carbonyl)amino]propanoate

Guidance literature:: Multi-step reaction with 5 steps

1: caesium carbonate; 1-{3,5-bis(trifluoromethyl)phenyl}-3-{(1R,2R)-2-(dimethylamino)cyclohexyl}thiourea / water; toluene / 144 h / -20 - 0 °C

2: formic acid / 20 h / 0 - 5 °C

3: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 0 °C

4: formic acid / 120 h / 20 °C

5: triethylamine / tetrahydrofuran / 4 h / 60 °C

With formic acid; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; 1-{3,5-bis(trifluoromethyl)phenyl}-3-{(1R,2R)-2-(dimethylamino)cyclohexyl}thiourea; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene;