methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

Base Information

Chemical Name:methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside
CAS No.:354986-46-2
Molecular Formula:C₃₀H₃₅NO₆
Molecular Weight:505.611
Hs Code.:

Synonyms:methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

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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 methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

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Technology Process of methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

There total 2 articles about methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside 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:

: 100-39-0
benzyl bromide

: 354986-46-2
methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / NaH / dimethylformamide / 15 h / 20 °C

2: 73 percent / NaBH₃CN; 1M HCl / diethyl ether; tetrahydrofuran / 2 h / 0 °C

With hydrogenchloride; sodium hydride; sodium cyanoborohydride; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/ja010086b

Reference yield:

: 6619-02-9,6619-04-1,10300-76-2,16727-56-3,17327-07-0,28978-56-5,52885-36-6,52885-45-7,78216-83-8,78513-50-5,87038-18-4,88295-36-7,110508-78-6,113159-04-9,117064-54-7,128657-61-4,129784-17-4,137330-28-0,78216-82-7
methyl N-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

: 354986-46-2
methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / NaH / dimethylformamide / 15 h / 20 °C

2: 73 percent / NaBH₃CN; 1M HCl / diethyl ether; tetrahydrofuran / 2 h / 0 °C

With hydrogenchloride; sodium hydride; sodium cyanoborohydride; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/ja010086b

Reference yield:

: 314740-77-7
2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranosyl triflate

: 354986-46-2
methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside

: methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-[2,3-di-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl]-(1->4)-α-D-glucopyranoside

Guidance literature:: 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranosyl triflate; methyl N-acetyl-N-benzyl-2-amino-2-deoxy-3,6-di-O-benzyl-α-D-glucopyranoside; In dichloromethane; at -78 - 0 ℃; for 4.5h;

With succinic acid anhydride; triethylamine; magnesium bromide; In dichloromethane; for 72h; Further stages.;
DOI:10.1021/ja010086b