Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester
CAS No.:206751-96-4
Molecular Formula:C₂₄H₂₉NO₇
Molecular Weight:443.497
Hs Code.:

Synonyms:Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

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Chemical Property of Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

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Technology Process of Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

There total 6 articles about Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl 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: 91.0%

: 206751-95-3
Acetic acid (2R,3S,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-3-yl ester

: 206751-96-4
Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; water; for 36h; Ambient temperature;
DOI:10.1016/S0008-6215(97)10017-9

Reference yield:

: 41355-95-7,347411-88-5
benzyl 2-acetamido-2-deoxy-β-D-galactopyranoside

: 206751-96-4
Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 76 percent / (+/-)-camphor-10-sulfonic acid / 48 h / Ambient temperature

2: 85 percent / BaO, Ba(OH)2*8H₂O / dimethylformamide / 20 h / Ambient temperature

3: 98 percent / acetic acid / H₂O / 0.67 h / 50 °C

4: 1.) imidazole, 2.) pyridine, 4-(dimethylamino)pyridine / 1.) DMF, 80 deg C, 2 h, 2.) room temperature, 2 h

5: 91 percent / HCl / tetrahydrofuran; H₂O / 36 h / Ambient temperature

With pyridine; 1H-imidazole; hydrogenchloride; dmap; barium dihydroxide; camphor-10-sulfonic acid; acetic acid; barium(II) oxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(97)10017-9

Reference yield:

: 100-39-0
benzyl bromide

: 206751-96-4
Acetic acid (2R,3R,4R,5R,6R)-5-acetylamino-6-benzyloxy-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / BaO, Ba(OH)2*8H₂O / dimethylformamide / 20 h / Ambient temperature

2: 98 percent / acetic acid / H₂O / 0.67 h / 50 °C

3: 1.) imidazole, 2.) pyridine, 4-(dimethylamino)pyridine / 1.) DMF, 80 deg C, 2 h, 2.) room temperature, 2 h

4: 91 percent / HCl / tetrahydrofuran; H₂O / 36 h / Ambient temperature

With pyridine; 1H-imidazole; hydrogenchloride; dmap; barium dihydroxide; acetic acid; barium(II) oxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(97)10017-9