Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

Base Information

Chemical Name:Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid
CAS No.:122116-48-7
Molecular Formula:C₄₁H₅₇NO₇
Molecular Weight:675.906
Hs Code.:

Synonyms:Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

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Technology Process of Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

There total 1 articles about Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid 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: 89.0%

: 101649-06-3
N-((R)-3-Benzyloxytetradecanoyloxy)succinimid

: 122116-46-5
Benzyl-2-amino-3-O-benzyl-2-desoxy-α-D-glucopyranosid

: 122116-48-7
Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; for 36h;

Reference yield:

: 122116-48-7
Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

: 122116-55-6
Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-6-O-<2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-β-D-glucopyranosyl>-2-desoxy-α-D-glucopyranosid

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) HgBr₂ , Hg(CN)2, moleculare sieve 4 Angstroem / 1.) CH₂Cl₂, 1 h, room temperature; 2.) CH₂Cl₂, 24 h

2: 98 percent / pyridine, 4-(dimethylamino)pyridine (DMAP) / 12 h / Ambient temperature

3: 95 percent / Zn-dust, glacial CH₃COOH / 1.5 h

4: 1.) EEDQ / 1.) CH₂Cl₂, 15 min; 2.) CH₂Cl₂, 24 h

5: 90 percent / pyridine, 1.4N NaOMe / methanol / 0.5 h

With pyridine; dmap; 4 A molecular sieve; sodium methylate; mercury(II) cyanide; acetic acid; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; mercury dibromide; zinc; In methanol;

Reference yield:

: 122116-48-7
Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-α-D-glucopyranosid

: 122116-56-7
Benzyl-3-O-benzyl-2-<(R)-3-benzyloxytetradecanoylamino>-6-O-<2-<(R)-3-benzyloxytetradecanoylamino>-2-desoxy-4,6-O-tetraisopropyldisiloxan-1,3-diyl-β-D-glucopyranosyl>-2-desoxy-α-D-glucopyranosid

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) HgBr₂ , Hg(CN)2, moleculare sieve 4 Angstroem / 1.) CH₂Cl₂, 1 h, room temperature; 2.) CH₂Cl₂, 24 h

2: 98 percent / pyridine, 4-(dimethylamino)pyridine (DMAP) / 12 h / Ambient temperature

3: 95 percent / Zn-dust, glacial CH₃COOH / 1.5 h

4: 1.) EEDQ / 1.) CH₂Cl₂, 15 min; 2.) CH₂Cl₂, 24 h

5: 90 percent / pyridine, 1.4N NaOMe / methanol / 0.5 h

6: pyridine / 2 h / Ambient temperature

With pyridine; dmap; 4 A molecular sieve; sodium methylate; mercury(II) cyanide; acetic acid; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; mercury dibromide; zinc; In methanol;