4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

Base Information

Chemical Name:4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol
CAS No.:850190-34-0
Molecular Formula:C₃₆H₄₇NO₅
Molecular Weight:573.773
Hs Code.:

Synonyms:4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

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Chemical Property of 4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

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Technology Process of 4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

There total 9 articles about 4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol 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: 78.0%

: 123-72-8
butyraldehyde

: 605675-59-0
4,5,7-tri-O-benzyl-1-O-butanoyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

: 850190-34-0
4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

Guidance literature:: With 4 A molecular sieve; sodium cyanoborohydride; acetic acid; In methanol; at 20 ℃;
DOI:10.1016/j.bmc.2004.12.043

Reference yield:

: 4,5,7-tri-O-benzyl-1,2,3-trideoxy-D-arabino-pept-1-enitol

: 850190-34-0
4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

Guidance literature:: Multi-step reaction with 8 steps

1: 87 percent / triphenylphosphine; diisopropyl azodicarboxylate / toluene / 20 °C

2: 91 percent / sodium / methanol / 4 h / 20 °C

3: 78 percent / triphenylphosphine; diisopropyl azodicarboxylate / toluene / 20 °C

4: ethylenediamine / ethanol / 80 °C

5: NIS / CH₂Cl₂ / 1 h / 20 °C

6: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 5 h / Heating

7: 82 percent / CH₂Cl₂ / 20 °C

8: 78 percent / glacial acetic acid; molecular sieves 4 Angstroem; NaBH₃CN / methanol / 20 °C

With N-iodo-succinimide; di-isopropyl azodicarboxylate; 4 A molecular sieve; sodium; sodium cyanoborohydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; ethylenediamine; triphenylphosphine; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; 1: Mitsunobu reaction / 3: Mitsunobu reaction;
DOI:10.1016/j.bmc.2004.12.043

Reference yield:

: 605675-52-3
(2R,3R,4R,6S)-3,4-di(benzyloxy)-2-benzyloxymethyl-1-azabicyclo[4.1.0]heptane

: 850190-34-0
4,5,7-tri-O-benzyl-1-O-butanoyl-N-butyl-2,3,6-trideoxy-2,6-imino-D-manno-heptitol

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / CH₂Cl₂ / 20 °C

2: 78 percent / glacial acetic acid; molecular sieves 4 Angstroem; NaBH₃CN / methanol / 20 °C

With 4 A molecular sieve; sodium cyanoborohydride; acetic acid; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2004.12.043