(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Base Information

Chemical Name:(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester
CAS No.:222848-24-0
Molecular Formula:C₅₃H₈₄N₆O₁₀
Molecular Weight:965.284
Hs Code.:

(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Synonyms:(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

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Chemical Property of (1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

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Technology Process of (1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

There total 6 articles about (1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl 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: 58.0%

: 2018-66-8
Z-Leu-OH

: 222848-11-5
(S)-2-Amino-N-((S)-1-{(4R,5R)-5-[(S)-1-((S)-2-amino-3-methyl-butyrylamino)-3-methyl-butyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-3-methyl-butyl)-3-methyl-butyramide

: 222848-24-0
(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In acetonitrile; at 20 ℃; for 0.25h;
DOI:10.1021/ja982893p

Reference yield:

: 1149-26-4
(S)-N-(benzyloxycarbonyl)valine

: 222848-24-0
(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / HBTU, Et₃N / acetonitrile / 0.25 h / 20 °C

2: 99 percent / H₂ / 10 percent Pd/C / ethyl acetate / 20 h / 20 °C / 760 Torr

3: 58 percent / HBTU, Et₃N / acetonitrile / 0.25 h / 20 °C

With hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; palladium on activated charcoal; In ethyl acetate; acetonitrile;
DOI:10.1021/ja982893p

Reference yield:

: 137649-68-4
(4-benzyloxycarbonylamino-2,3-dihydroxy-1-isobutyl-6-methyl-heptyl)-carbamic acid benzyl ester

: 222848-24-0
(1-{1-[1-(5-{1-[2-(2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-3-methyl-butyl}-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 96 percent / p-TsOH / 5 h / 60 °C

2: 93 percent / H₂ / 10 percent Pd/C / ethyl acetate / 20 h / 20 °C / 760 Torr

3: 82 percent / HBTU, Et₃N / acetonitrile / 0.25 h / 20 °C

4: 99 percent / H₂ / 10 percent Pd/C / ethyl acetate / 20 h / 20 °C / 760 Torr

5: 58 percent / HBTU, Et₃N / acetonitrile / 0.25 h / 20 °C

With hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; toluene-4-sulfonic acid; triethylamine; palladium on activated charcoal; In ethyl acetate; acetonitrile;
DOI:10.1021/ja982893p