{3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

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Chemical Name:{3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester
CAS No.:253590-88-4
Molecular Formula:C₂₉H₄₀N₂O₇
Molecular Weight:528.646
Hs Code.:

Synonyms:{3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

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Chemical Property of {3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

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Technology Process of {3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

There total 4 articles about {3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl 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: 90.0%

: 253590-70-4
1,3-di[N-(4-methoxybenzyl)-N-[(isobutyloxy)carbonyl]amino]-2-hydroxypropane

: 253590-88-4
{3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

Guidance literature:: With sodium hypochlorite; sodium hydrogencarbonate; potassium bromide; 2,2,6,6-tetramethyl-piperidine-N-oxyl; In dichloromethane; water; at 0 - 20 ℃;
DOI:10.1016/S0223-5234(00)80031-8

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 253590-88-4
{3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: Na₂SO₄ / CH₂Cl₂ / 20 °C

2: NaBH₄ / ethanol / 20 °C

3: 98 percent / Et₃N / CH₂Cl₂ / 0 - 20 °C

4: 90 percent / NaOCl; sat. NaHCO₃; KBr / TEMPO / CH₂Cl₂; H₂O / 0 - 20 °C

With sodium hypochlorite; sodium tetrahydroborate; sodium hydrogencarbonate; sodium sulfate; triethylamine; potassium bromide; 2,2,6,6-tetramethyl-piperidine-N-oxyl; In ethanol; dichloromethane; water; 1: Condensation / 2: Reduction / 3: Carboxylation / 4: Oxidation;
DOI:10.1016/S0223-5234(00)80031-8

Reference yield:

: 1,3-bis[(E)-(4-methoxybenzylidene)amino] propan-2-ol

: 253590-88-4
{3-[isobutoxycarbonyl-(4-methoxy-benzyl)-amino]-2-oxo-propyl}-(4-methoxy-benzyl)-carbamic acid isobutyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: NaBH₄ / ethanol / 20 °C

2: 98 percent / Et₃N / CH₂Cl₂ / 0 - 20 °C

3: 90 percent / NaOCl; sat. NaHCO₃; KBr / TEMPO / CH₂Cl₂; H₂O / 0 - 20 °C

With sodium hypochlorite; sodium tetrahydroborate; sodium hydrogencarbonate; triethylamine; potassium bromide; 2,2,6,6-tetramethyl-piperidine-N-oxyl; In ethanol; dichloromethane; water; 1: Reduction / 2: Carboxylation / 3: Oxidation;
DOI:10.1016/S0223-5234(00)80031-8