3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

Base Information

Chemical Name:3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose
CAS No.:667923-26-4
Molecular Formula:C₂₅H₃₀N₂O₆S
Molecular Weight:486.589
Hs Code.:

Synonyms:3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

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Chemical Property of 3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

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Technology Process of 3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

There total 3 articles about 3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose 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: 62.0%

: 100-39-0
benzyl bromide

: 667923-22-0
Ethanesulfonic acid ((3aR,5S,6R,6aR)-5-benzyloxymethyl-6-cyano-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-amide

: 667923-26-4
3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

Guidance literature:: With potassium carbonate; In acetone; for 3h; Heating;
DOI:10.1021/jo035301g

Reference yield:

: 34311-63-2
5-O-benzyl-3-oxo-1,2-O-isopropylidene-α-D-xylofuranose

: 667923-26-4
3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

Guidance literature:: Multi-step reaction with 3 steps

1.1: Ti(OiPr)4; NH₃ / methanol / 5 h / 20 °C

1.2: 70 percent / methanol / 12 h / 20 °C

2.1: pyridine / 2 h / 20 °C

3.1: 62 percent / K₂CO₃ / acetone / 3 h / Heating

With pyridine; titanium(IV) isopropylate; ammonia; potassium carbonate; In methanol; acetone;
DOI:10.1021/jo035301g

Reference yield:

: 302582-09-8
3-amino-5-O-benzyl-3-C-cyano-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose

: 667923-26-4
3-amino-3-N-benzyl-5-O-benzyl-3-C-cyano-3-deoxy-3-N-ethanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 2 h / 20 °C

2: 62 percent / K₂CO₃ / acetone / 3 h / Heating

With pyridine; potassium carbonate; In acetone;
DOI:10.1021/jo035301g