3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

Base Information

• Chemical Name: 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester
• CAS No.: 210355-29-6
• Molecular Formula: C₆₀H₉₀N₆O₁₈
• Molecular Weight: 1183.4
• Mol file: 210355-29-6.mol

Synonyms:3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

Chemical Property of 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

There total 4 articles about 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl 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:

1-carbomethoxy-3,5-dihydroxybenzene (2150-44-9) → 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester (210355-29-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 30 percent / 1.) Na; 2.) 5 molpercent benzyltriethylammonium chloride / 1.) MeOH; 2.) reflux, 36 h

2: 80 percent / 25percent HCl, hydrogen / PtO₂ / methanol / 10 h / 3000.2 Torr

3: 1.) carbonyldiimidazole; 2.) 1,8-diazabicyclo<5.4.0>undec-7-ene / 1.) dichloromethane, 12 h; 2.) dichloromethane, 12 h

With hydrogenchloride; N-benzyl-N,N,N-triethylammonium chloride; hydrogen; sodium; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1,1'-carbonyldiimidazole; platinum(IV) oxide; In methanol;

DOI:10.1002/(SICI)1099-0690(199807)1998:7<1275::AID-EJOC1275>3.0.CO;2-2

Reference yield:

3,5-Bis-(2-cyano-ethoxy)-benzoic acid methyl ester (210355-15-0) → 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester (210355-29-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / 25percent HCl, hydrogen / PtO₂ / methanol / 10 h / 3000.2 Torr

2: 1.) carbonyldiimidazole; 2.) 1,8-diazabicyclo<5.4.0>undec-7-ene / 1.) dichloromethane, 12 h; 2.) dichloromethane, 12 h

With hydrogenchloride; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1,1'-carbonyldiimidazole; platinum(IV) oxide; In methanol;

DOI:10.1002/(SICI)1099-0690(199807)1998:7<1275::AID-EJOC1275>3.0.CO;2-2

Reference yield:

methyl 3,5‐bis(3‐((tert‐butoxycarbonyl)amino)propoxy)benzoate (210355-19-4) → 3,5-Bis-{3-[3,5-bis-(3-tert-butoxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester (210355-29-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / potassium hydroxide / methanol; H₂O / 2 h / Heating

2: 1.) carbonyldiimidazole; 2.) 1,8-diazabicyclo<5.4.0>undec-7-ene / 1.) dichloromethane, 12 h; 2.) dichloromethane, 12 h

With potassium hydroxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1,1'-carbonyldiimidazole; In methanol; water;

DOI:10.1002/(SICI)1099-0690(199807)1998:7<1275::AID-EJOC1275>3.0.CO;2-2

upstream raw materials:

3,5‐bis(3‐((tert‐butoxycarbonyl)amino)propoxy)benzoic acid

1-carbomethoxy-3,5-dihydroxybenzene

3,5-Bis-(2-cyano-ethoxy)-benzoic acid methyl ester

methyl 3,5‐bis(3‐((tert‐butoxycarbonyl)amino)propoxy)benzoate