((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

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Chemical Name:((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester
CAS No.:263247-21-8
Molecular Formula:C₃₂H₄₇NO₈S₂
Molecular Weight:637.859
Hs Code.:

Synonyms:((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

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Chemical Property of ((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

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Technology Process of ((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

There total 8 articles about ((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester 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:

: 110-87-2
3,4-dihydro-2H-pyran

: 263247-21-8
((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / BF₃*OEt₂ / CH₂Cl₂

2: 84 percent / (i-Pr)2NEt; DMAP / CH₂Cl₂

3: 64 percent / n-BuLi; CuI / tetrahydrofuran / -78 °C

4: LiAlH₄ / diethyl ether

5: Et₃N; DMAP / CH₂Cl₂

With dmap; copper(l) iodide; lithium aluminium tetrahydride; n-butyllithium; boron trifluoride diethyl etherate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane; 1: Addition / 2: Etherification / 3: Alkylation / 4: Reduction / 5: Acylation;
DOI:10.3987/com-99-s82

Reference yield:

: 57795-10-5
5-(1',3'-dithian-2'-yl)-1-pentanol

: 263247-21-8
((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / (i-Pr)2NEt; DMAP / CH₂Cl₂

2: 64 percent / n-BuLi; CuI / tetrahydrofuran / -78 °C

3: LiAlH₄ / diethyl ether

4: Et₃N; DMAP / CH₂Cl₂

With dmap; copper(l) iodide; lithium aluminium tetrahydride; n-butyllithium; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane; 1: Etherification / 2: Alkylation / 3: Reduction / 4: Acylation;
DOI:10.3987/com-99-s82

Reference yield:

: 105363-12-0
N-hydroxy-3,4-dimethoxybenzenecarboximidoyl chloride

: 263247-21-8
((1S,3R)-1-(3,4-Dimethoxy-phenyl)-3-hydroxy-4-{2-[4-(2-methoxy-ethoxymethoxy)-butyl]-[1,3]dithian-2-yl}-butyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: Et₂Zn; (R,R)-DIPT; 1,4-dioxane / CHCl₃ / 0 °C

2: 92 percent / Et₃N / CH₂Cl₂

3: 64 percent / n-BuLi; CuI / tetrahydrofuran / -78 °C

4: LiAlH₄ / diethyl ether

5: Et₃N; DMAP / CH₂Cl₂

With 1,4-dioxane; dmap; copper(l) iodide; lithium aluminium tetrahydride; n-butyllithium; L-(+)-diisopropyl tartrate; diethylzinc; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; chloroform; 1: Cycloaddition / 2: Esterification / 3: Alkylation / 4: Reduction / 5: Acylation;
DOI:10.3987/com-99-s82