(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

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Chemical Name:(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester
CAS No.:214051-77-1
Molecular Formula:C₅₅H₇₀N₄O₁₁
Molecular Weight:963.181
Hs Code.:

(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

Synonyms:(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

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Chemical Property of (S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

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Technology Process of (S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

There total 1 articles about (S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric 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: 83.0%

: 13518-40-6
L-valine tert-butylester hydrochloride

: 189280-27-1
(2S,9R)-11-[(Benzyloxycarbonyl)amino]-7-(carbobenzyloxy)-2-[(9-fluorenylmethoxycarbonyl)amino]-9-(tetrahydropyran-2-yloxy)-7-azaundecanoic Acid

: 214051-77-1
(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 21h; Ambient temperature;
DOI:10.1021/jm980389p

Reference yield: 89.0%

: 214051-77-1
(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

: 214051-78-2
(S)-2-((S)-2-Amino-6-{benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-hexanoylamino)-3-methyl-butyric acid tert-butyl ester

Guidance literature:: With piperidine; In N,N-dimethyl-formamide; for 4.5h;
DOI:10.1021/jm980389p

Reference yield:

: 214051-77-1
(S)-2-[(S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-(tetrahydro-pyran-2-yloxy)-butyl]-amino}-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-3-methyl-butyric acid tert-butyl ester

: (S)-2-((S)-6-{Benzyloxycarbonyl-[(R)-4-benzyloxycarbonylamino-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-butyl]-amino}-2-tert-butoxycarbonylamino-hexanoylamino)-3-methyl-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / piperidine / dimethylformamide / 4.5 h

2: 82 percent / p-toluenesulfonic acid / acetone; H₂O / 2 h / 45 °C

3: 99 percent / dioxane; H₂O / 5 h / Ambient temperature

4: 78 percent / pyridine / CCl₄ / 17 h / Ambient temperature

With piperidine; pyridine; toluene-4-sulfonic acid; In 1,4-dioxane; tetrachloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm980389p