(S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

Base Information

Chemical Name:(S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid
CAS No.:521274-09-9
Molecular Formula:C₄₂H₄₅N₃O₈
Molecular Weight:719.835
Hs Code.:

Synonyms:(S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

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Chemical Property of (S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

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Technology Process of (S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

There total 9 articles about (S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid 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:

: 883-99-8
3-hydroxy-2-naphthoic acid methyl ester

: 521274-09-9
(S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 56 percent / Ph₃P; diethylazodicarboxylate / tetrahydrofuran / 15 h / 0 - 20 °C

2.1: 95 percent / aq. HCl / dioxane / 1.75 h / 20 °C

3.1: EDCI; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 0.17 h / 20 °C

3.2: 52 percent / CH₂Cl₂ / 19 h / 20 °C

4.1: 16 mg / Cu(OAc)2 / propan-2-ol / 17 h / Heating

With 4-methyl-morpholine; hydrogenchloride; copper diacetate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; isopropyl alcohol; 1.1: Mitsunobu reaction;
DOI:10.1021/ja0296733

Reference yield:

: 2298-07-9
4-Bromo-1-naphthylamine

: 521274-09-9
(S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: Zn / dimethylformamide / 0.25 h / 65 °C

1.2: 46 percent / Pd(OAc)2; tris(o-tolyl)phosphine / dimethylformamide / 1.5 h / 65 °C

2.1: 91 percent / aq. NaOH / methanol / 2.5 h / 20 °C

3.1: EDCI; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 0.17 h / 20 °C

3.2: 52 percent / CH₂Cl₂ / 19 h / 20 °C

4.1: 16 mg / Cu(OAc)2 / propan-2-ol / 17 h / Heating

With 4-methyl-morpholine; sodium hydroxide; copper diacetate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; zinc; In methanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/ja0296733

Reference yield:

: 75178-90-4
N-(tert-butyloxycarbonyl)-5-aminopentanol

: 521274-09-9
(S)-3-{{5-[[2-(tert-butoxycarbonylamino)-3-[4-((2-carboxyphenyl)amino)naphthalen-1-yl]propionyl]amino]pentyl}oxy}naphthalene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 56 percent / Ph₃P; diethylazodicarboxylate / tetrahydrofuran / 15 h / 0 - 20 °C

2.1: 95 percent / aq. HCl / dioxane / 1.75 h / 20 °C

3.1: EDCI; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 0.17 h / 20 °C

3.2: 52 percent / CH₂Cl₂ / 19 h / 20 °C

4.1: 16 mg / Cu(OAc)2 / propan-2-ol / 17 h / Heating

With 4-methyl-morpholine; hydrogenchloride; copper diacetate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; isopropyl alcohol; 1.1: Mitsunobu reaction;
DOI:10.1021/ja0296733