(6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

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Chemical Name:(6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester
CAS No.:239064-34-7
Molecular Formula:C₃₇H₆₂N₄O₆
Molecular Weight:658.922
Hs Code.:

(6-{[2-(2-<i>tert</i>-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:(6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

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Chemical Property of (6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

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Technology Process of (6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

There total 7 articles about (6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-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: 91.0%

: 55721-65-8
Boc-D-Ile-OH

: 239064-33-6
{6-[(2-amino-3-phenyl-propionyl)-cyclohexyl-amino]-hexyl}-carbamic acid tert-butyl ester

: 239064-34-7
(6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In N,N-dimethyl-formamide; for 4h;
DOI:10.1021/jm990110k

Reference yield:

: 4048-33-3
6-amino-1-hexanol

: 239064-34-7
(6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 88 percent / dioxane; H₂O / 12 h / Ambient temperature

2: 91 percent / pyridinium chlorochromate, neutal alumina / CH₂Cl₂ / 3 h / Ambient temperature

3: 25 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / 3 h / Ambient temperature

4: diisopropylethylamine / CH₂Cl₂ / 18 h / Heating

5: 67 percent / piperidine / dimethylformamide / 0.25 h / Ambient temperature

6: 91 percent / HOBt, EDC, 4-methylmorpholine / dimethylformamide / 4 h

With piperidine; 4-methyl-morpholine; aluminum oxide; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; In 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/jm990110k

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 239064-34-7
(6-{[2-(2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-3-phenyl-propionyl]-cyclohexyl-amino}-hexyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 88 percent / dioxane; H₂O / 12 h / Ambient temperature

2: 91 percent / pyridinium chlorochromate, neutal alumina / CH₂Cl₂ / 3 h / Ambient temperature

3: 25 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / 3 h / Ambient temperature

4: diisopropylethylamine / CH₂Cl₂ / 18 h / Heating

5: 67 percent / piperidine / dimethylformamide / 0.25 h / Ambient temperature

6: 91 percent / HOBt, EDC, 4-methylmorpholine / dimethylformamide / 4 h

With piperidine; 4-methyl-morpholine; aluminum oxide; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; In 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/jm990110k