<5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

Base Information

Chemical Name:<5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin
CAS No.:133886-16-5
Molecular Formula:C₂₆H₃₂N₂O₈
Molecular Weight:500.549
Hs Code.:

Synonyms:<5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

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Chemical Property of <5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

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Technology Process of <5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

There total 6 articles about <5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin 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: 72.0%

: 129829-37-4
<5R,1'R,2'R,3'S>-5-(1'-t-Butyldimethylsilyloxy-2',3'-O-isopropylidenedioxy-4'-benzyloxy)butyl-5-methoxy-3-(4-methoxybenzyl)hydantoin

: 133886-16-5
<5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.666667h;
DOI:10.1016/S0040-4020(01)96123-X

Reference yield:

: 5-Bromo-1-(tert-butyl-dimethyl-silanyl)-3-(4-methoxy-benzyl)-imidazolidine-2,4-dione

: 133886-16-5
<5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / CCl₄ / 1 h / 0 °C

3: 12 percent / 0.5M aq. K₂CO₃ / methanol / 80 h / Ambient temperature

4: 72 percent / n-Bu₄NF / tetrahydrofuran / 0.67 h / 0 °C

With tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; tetrachloromethane;
DOI:10.1016/S0040-4020(01)96123-X

Reference yield:

: 133886-09-6
1-t-Butyldimethylsilyl-5-methoxy-3-(4-methoxybenzyl)hydantoin

: 133886-16-5
<5R,1'R,2'R,3'S>-5-(4'-benzyloxy-2',3'-O-isopropylidenedioxy-1'-hydroxy)butyl-5-methoxy-3-N-(4-methoxybenzyl)hydantoin

Guidance literature:: Multi-step reaction with 3 steps

2: 12 percent / 0.5M aq. K₂CO₃ / methanol / 80 h / Ambient temperature

3: 72 percent / n-Bu₄NF / tetrahydrofuran / 0.67 h / 0 °C

With tetrabutyl ammonium fluoride; potassium carbonate; In tetrahydrofuran; methanol;
DOI:10.1016/S0040-4020(01)96123-X