1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

Base Information

Chemical Name:1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside
CAS No.:1334216-64-6
Molecular Formula:C₂₄H₃₃NO₇
Molecular Weight:447.529
Hs Code.:

Synonyms:1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

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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 1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

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Technology Process of 1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

There total 6 articles about 1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside 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: 99.0%

: 1334216-54-4
1-C-allyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

: 108-24-7
acetic anhydride

: 1334216-64-6
1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

Guidance literature:: With dmap; at 0 - 20 ℃;
DOI:10.1002/ejoc.201100533

Reference yield:

: (1S,5R,6R,8R)-8-allyl-3,3-dimethyl-6-hydroxymethyl-2,4,7-trioxabicyclo[3.3.0]octane

: 1334216-64-6
1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: 0 - 60 °C / Inert atmosphere

3: sodium carbonate / tetrahydrofuran; water / 0 - 20 °C

4: hydrogenchloride; water / tetrahydrofuran / 18 h / 50 °C

5: dmap / 0 - 20 °C

With hydrogenchloride; dmap; water; sodium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1002/ejoc.201100533

Reference yield:

: 1334216-52-2
1-C-allyl-2,3-O-isopropylidene-5-O-mesyl-α-D-ribofuranoside

: 1334216-64-6
1-C-allyl-2,3-di-O-acetyl-5-(N-n-butyl-N-Cbz)amino-5-deoxy-α-D-ribofuranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 0 - 60 °C / Inert atmosphere

2: sodium carbonate / tetrahydrofuran; water / 0 - 20 °C

3: hydrogenchloride; water / tetrahydrofuran / 18 h / 50 °C

4: dmap / 0 - 20 °C

With hydrogenchloride; dmap; water; sodium carbonate; In tetrahydrofuran; water;
DOI:10.1002/ejoc.201100533