4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

Base Information

Chemical Name:4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose
CAS No.:1603836-22-1
Molecular Formula:C₃₅H₅₆N₄O₇Si₂
Molecular Weight:701.023
Hs Code.:

Synonyms:4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

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Chemical Property of 4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

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Technology Process of 4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

There total 9 articles about 4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose 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: 43.0%

: 1603836-13-0
4S-{(1R,8S,11R)-9-N-benzyl-3-N-(2-cyanoethyl)-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

: 1603836-22-1
4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1h;
DOI:10.1002/ejoc.201400140

Reference yield: 43.0%

: 4R-{9-N-benzyl-3-N-(2-cyanoethyl)-3,9-diaza-10-oxa-2-oxobicyclo[6.3.0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythrofuranose

: 1603836-22-1
4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

: 1603836-23-2
4S-{(1S,8R,11S)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo-[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-deoxy-1-(uracil-1-yl)-β-D-erythro-furanose

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1h;
DOI:10.1002/ejoc.201400140

Reference yield:

: 161867-43-2
(2S,3R,4R,5R)-3,4-bis(tert-butyldimethylsilanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydrofuran-2-carbaldehyde

: 1603836-22-1
4S-{(1R,8S,11R)-9-N-benzyl-3,9-diaza-10-oxa-2-oxobicylo[6,3,0]undecan-11-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

Guidance literature:: Multi-step reaction with 4 steps

1.1: zinc trifluoromethanesulfonate; N,N,N,N,-tetramethylethylenediamine; triethylamine / tetrahydrofuran / 0.17 h / 20 °C

1.2: 48 h / 20 °C

2.1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dimethyl sulfoxide; acetonitrile / 3 h / 20 °C

3.1: acetonitrile / 96 h / Molecular sieve; Reflux

4.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C

With N,N,N,N,-tetramethylethylenediamine; potassium tert-butylate; zinc trifluoromethanesulfonate; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dimethyl sulfoxide; acetonitrile; 1.1: |Horner-Wadsworth-Emmons Olefination / 1.2: |Horner-Wadsworth-Emmons Olefination;
DOI:10.1002/ejoc.201400140