(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

Base Information

Chemical Name:(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane
CAS No.:716371-63-0
Molecular Formula:C₄₁H₆₉N₃O₇Si
Molecular Weight:744.1
Hs Code.:

(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

Synonyms:(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

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Chemical Property of (1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

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Technology Process of (1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

There total 9 articles about (1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane 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: 60.0%

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

: (S)-2-Amino-N-[(1S,2R)-1-((S)-sec-butyl)-2-methoxy-4-oxo-4-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-butyl]-3,N-dimethyl-butyramide

: 716371-63-0
(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

Guidance literature:: With bromo-tris-dimethylamino-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/jo0497499

Reference yield:

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

: 716371-63-0
(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / diisopropylethylamine; bromotris(dimethylamino)phosphonium hexafluorophosphate / CH₂Cl₂ / 24 h / 20 °C

2: 99 percent / H₂ / Pd/C / ethyl acetate / 25 °C / balloon

3: 60 percent / diisopropylethylamine; bromotris(dimethylamino)phosphonium hexafluorophosphate / CH₂Cl₂ / 24 h / 20 °C

With bromo-tris-dimethylamino-phosphonium hexafluorophosphate; hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1021/jo0497499

Reference yield:

: 120205-56-3
benzyl methyl[(2S,3S)-3-methyl-1-oxopentan-2-yl]carbamate

: 716371-63-0
(1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C

1.2: 75 percent / hexane; tetrahydrofuran / 0.5 h / -78 °C

2.1: 75 percent / molecular sieves 4 Angstroem / CH₂Cl₂ / 24 h / 20 °C

3.1: 99 percent / H₂ / Pd/C / ethyl acetate / 25 °C / balloon

4.1: 81 percent / diisopropylethylamine; bromotris(dimethylamino)phosphonium hexafluorophosphate / CH₂Cl₂ / 24 h / 20 °C

5.1: 99 percent / H₂ / Pd/C / ethyl acetate / 25 °C / balloon

6.1: 60 percent / diisopropylethylamine; bromotris(dimethylamino)phosphonium hexafluorophosphate / CH₂Cl₂ / 24 h / 20 °C

With n-butyllithium; bromo-tris-dimethylamino-phosphonium hexafluorophosphate; 4 A molecular sieve; hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; hexane; dichloromethane; ethyl acetate;
DOI:10.1021/jo0497499