[5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

Base Information

Chemical Name:[5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester
CAS No.:891090-44-1
Molecular Formula:C₄₂H₇₃N₅O₈
Molecular Weight:776.07
Hs Code.:

Synonyms:[5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

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Chemical Property of [5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

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Technology Process of [5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

There total 7 articles about [5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl 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: 87.0%

: 891090-20-3
N-stearyl-4-(aminomethyl)-3-nitrobenzamide

: 2483-46-7
Boc-Lys(Boc)-OH

: 891090-44-1
[5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1039/b518359f

Reference yield:

: 130029-61-7
4-[[(2,2,2-trifluoroacetyl)amino]methyl]benzoic acid

: 891090-44-1
[5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 92 percent / aq. nitric acid / 1.5 h / 0 °C

2: K₂CO₃; H₂O / methanol / 10 h / 25 °C

3: 0.67 g / dioxane; H₂O / 2.5 h

4: 81 percent / HOBT; Et₃N; HBTU / CHCl₃ / 10 h / 20 °C

5: 94 percent / HCl / dioxane / 3 h / 20 °C

6: 87 percent / HOBT; HBTU; N-methylmorpholine / dimethylformamide / 20 °C

With 4-methyl-morpholine; hydrogenchloride; water; nitric acid; potassium carbonate; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In 1,4-dioxane; methanol; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1039/b518359f

Reference yield:

: 56-91-7
p-aminomethylbenzoic acid

: 891090-44-1
[5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 88 percent / 2 h / 25 °C

2: 92 percent / aq. nitric acid / 1.5 h / 0 °C

3: K₂CO₃; H₂O / methanol / 10 h / 25 °C

4: 0.67 g / dioxane; H₂O / 2.5 h

5: 81 percent / HOBT; Et₃N; HBTU / CHCl₃ / 10 h / 20 °C

6: 94 percent / HCl / dioxane / 3 h / 20 °C

7: 87 percent / HOBT; HBTU; N-methylmorpholine / dimethylformamide / 20 °C

With 4-methyl-morpholine; hydrogenchloride; water; nitric acid; potassium carbonate; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In 1,4-dioxane; methanol; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1039/b518359f