(2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

Base Information

Chemical Name:(2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid
CAS No.:676241-07-9
Molecular Formula:C₂₈H₂₉N₃O₆
Molecular Weight:503.555
Hs Code.:

Synonyms:(2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

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Chemical Property of (2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

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Technology Process of (2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

There total 6 articles about (2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid 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: 100.0%

: 676241-06-8
tert-butyl 2,6-anhydro-7-azido-3,4,5-tri-O-benzyl-7-deoxy-L-glycero-L-gluco-hepturonate

: 676241-07-9
(2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 20h;
DOI:10.1016/j.tetlet.2003.12.032

Reference yield:

: 112219-66-6
(2R,3R,4R,5S,6S)-3,4,5-tris(benzyloxy)-2-(benzyloxymethyl)-6-vinyltetrahydro-2H-pyran

: 676241-07-9
(2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -40 °C

2.1: sodium methylate / methanol / 20 h / 20 °C

3.1: acetic anhydride; pyridinium chlorochromate / dichloromethane / 48 h / 20 °C

4.1: ozone / dichloromethane / 0.5 h / -78 °C

4.2: NaBH₄ / 11; 15 / 20 h / 20 °C

5.1: triethylamine / dichloromethane / 20 h / 20 °C

6.1: sodium azide / N,N-dimethyl-formamide / 20 h / 90 °C

7.1: trifluoroacetic acid / dichloromethane / 20 h / 20 °C

With sodium azide; trimethylsilyl trifluoromethanesulfonate; sodium methylate; acetic anhydride; ozone; triethylamine; pyridinium chlorochromate; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide; 2.1: Zemplen deacetylation;
DOI:10.1016/j.tetlet.2003.12.032

Reference yield:

: 676241-03-5
((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-6-vinyl-tetrahydro-pyran-2-yl)-methanol

: 676241-07-9
(2S,3S,4R,5S,6S)-6-Azidomethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetic anhydride; pyridinium chlorochromate / dichloromethane / 48 h / 20 °C

2.1: ozone / dichloromethane / 0.5 h / -78 °C

2.2: NaBH₄ / 11; 15 / 20 h / 20 °C

3.1: triethylamine / dichloromethane / 20 h / 20 °C

4.1: sodium azide / N,N-dimethyl-formamide / 20 h / 90 °C

5.1: trifluoroacetic acid / dichloromethane / 20 h / 20 °C

With sodium azide; acetic anhydride; ozone; triethylamine; pyridinium chlorochromate; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2003.12.032