2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

Base Information

Chemical Name:2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester
CAS No.:243657-80-9
Molecular Formula:C₃₁H₃₁NO₉
Molecular Weight:561.588
Hs Code.:

2-<i>tert</i>-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4<i>H</i>-chromen-7-yl ester

Synonyms:2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

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Chemical Property of 2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

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Technology Process of 2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

There total 5 articles about 2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl 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: 81.0%

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 243657-83-2
5,7-dihydroxy-3-(4-methoxy-phenoxy)-2-methyl-chromen-4-one

: 243657-80-9
2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

Guidance literature:: N-tert-butoxycarbonyl-L-phenylalanine; With dicyclohexyl-carbodiimide; In tetrahydrofuran; at 0 ℃; for 0.5h;

5,7-dihydroxy-3-(4-methoxy-phenoxy)-2-methyl-chromen-4-one; With dmap; In tetrahydrofuran; at 0 ℃; for 0.5h;
DOI:10.1007/BF02329590

Reference yield:

: 108-73-6
3,5-dihydroxyphenol

: 243657-80-9
2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: HCl gas; ZnCl₂ / benzene; diethyl ether / 24 h / 0 - 5 °C

1.2: 78 percent / aq. H₂SO₄ / 2 h / Heating

2.1: 89 percent / Et₃N; NaOAc / 4 h / 130 - 140 °C

3.1: 83 percent / HCl / ethanol / Heating

4.1: DCC / tetrahydrofuran / 0.5 h / 0 °C

4.2: 81 percent / DMAP / tetrahydrofuran / 0.5 h / 0 °C

With hydrogenchloride; sodium acetate; triethylamine; dicyclohexyl-carbodiimide; zinc(II) chloride; In tetrahydrofuran; diethyl ether; ethanol; benzene; 1.1: Condensation / 1.2: Hydrolysis / 2.1: Cyclization / 3.1: Hydrolysis / 4.1: Substitution / 4.2: Acylation;
DOI:10.1007/BF02329590

Reference yield:

: 22446-12-4
2-(4-methoxyphenoxy)acetonitrile

: 243657-80-9
2-tert-butoxycarbonylamino-3-phenyl-propionic acid 5-hydroxy-3-(4-methoxy-phenoxy)-2-methyl-4-oxo-4H-chromen-7-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: HCl gas; ZnCl₂ / benzene; diethyl ether / 24 h / 0 - 5 °C

1.2: 78 percent / aq. H₂SO₄ / 2 h / Heating

2.1: 89 percent / Et₃N; NaOAc / 4 h / 130 - 140 °C

3.1: 83 percent / HCl / ethanol / Heating

4.1: DCC / tetrahydrofuran / 0.5 h / 0 °C

4.2: 81 percent / DMAP / tetrahydrofuran / 0.5 h / 0 °C

With hydrogenchloride; sodium acetate; triethylamine; dicyclohexyl-carbodiimide; zinc(II) chloride; In tetrahydrofuran; diethyl ether; ethanol; benzene; 1.1: Condensation / 1.2: Hydrolysis / 2.1: Cyclization / 3.1: Hydrolysis / 4.1: Substitution / 4.2: Acylation;
DOI:10.1007/BF02329590