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

Base Information

Chemical Name:3,5-Bis-{3-[3,5-bis-(3-benzyloxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester
CAS No.:210355-28-5
Molecular Formula:C₇₂H₈₂N₆O₁₈
Molecular Weight:1319.47
Hs Code.:

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

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

Chemical Property:

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

There total 6 articles about 3,5-Bis-{3-[3,5-bis-(3-benzyloxycarbonylamino-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:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 210355-28-5
3,5-Bis-{3-[3,5-bis-(3-benzyloxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 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: 86 percent / potassium hydroxide / tetrahydrofuran; H₂O / 2 h / 0 °C

4: 85 percent / potassium hydroxide / methanol / 2 h / Heating

5: 1.) carbonyldiimidazole; 2.) triethylamine / 1.) acetonitrile, 12 h; 2.) acetonitrile, 12 h

With hydrogenchloride; potassium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; hydrogen; sodium; triethylamine; 1,1'-carbonyldiimidazole; platinum(IV) oxide; In tetrahydrofuran; methanol; water;
DOI:10.1002/(SICI)1099-0690(199807)1998:7<1275::AID-EJOC1275>3.0.CO;2-2

Reference yield:

: 210355-15-0
3,5-Bis-(2-cyano-ethoxy)-benzoic acid methyl ester

: 210355-28-5
3,5-Bis-{3-[3,5-bis-(3-benzyloxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

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

2: 86 percent / potassium hydroxide / tetrahydrofuran; H₂O / 2 h / 0 °C

3: 85 percent / potassium hydroxide / methanol / 2 h / Heating

4: 1.) carbonyldiimidazole; 2.) triethylamine / 1.) acetonitrile, 12 h; 2.) acetonitrile, 12 h

With hydrogenchloride; potassium hydroxide; hydrogen; triethylamine; 1,1'-carbonyldiimidazole; platinum(IV) oxide; In tetrahydrofuran; methanol; water;
DOI:10.1002/(SICI)1099-0690(199807)1998:7<1275::AID-EJOC1275>3.0.CO;2-2

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 210355-28-5
3,5-Bis-{3-[3,5-bis-(3-benzyloxycarbonylamino-propoxy)-benzoylamino]-propoxy}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / potassium hydroxide / tetrahydrofuran; H₂O / 2 h / 0 °C

2: 85 percent / potassium hydroxide / methanol / 2 h / Heating

3: 1.) carbonyldiimidazole; 2.) triethylamine / 1.) acetonitrile, 12 h; 2.) acetonitrile, 12 h

With potassium hydroxide; triethylamine; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; water;
DOI:10.1002/(SICI)1099-0690(199807)1998:7<1275::AID-EJOC1275>3.0.CO;2-2