2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

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Chemical Name:2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester
CAS No.:295337-51-8
Molecular Formula:C₅₃H₇₁NO₁₁SSi
Molecular Weight:958.298
Hs Code.:

2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

Synonyms:2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

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Chemical Property of 2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

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Technology Process of 2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

There total 8 articles about 2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl 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: 83.0%

: 108-59-8
malonic acid dimethyl ester

: 295337-49-4
N-[2-(6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-1-(4-iodo-butoxymethyl)-ethyl]-N-[5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-4-methyl-benzenesulfonamide

: 295337-51-8
2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

Guidance literature:: With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1016/S0040-4039(00)00710-3

Reference yield:

: 194861-23-9
2-((benzyloxy)methyl)-3,4-dihydro-2H-pyran

: 295337-51-8
2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridinium p-toluenesulfonate / 1,2-dichloro-ethane / 16 h / 75 °C

2.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 3 h / 20 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C

4.1: 2,6-di-tert-butyl-pyridine; silver trifluoromethanesulfonate / dichloromethane / 4 h / 20 °C

4.2: DDQ / 22; 15 / 4 h / 20 °C

5.1: 1H-imidazole; iodine; triphenylphosphine / toluene; acetonitrile / 10 h / 20 °C

6.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide / 12 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; 2,6-di-tert-butyl-pyridine; iodine; silver trifluoromethanesulfonate; pyridinium p-toluenesulfonate; sodium hydride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene; acetonitrile; 1.1: Etherification / 2.1: Mitsunobu reaction / 3.1: Reduction / 4.1: Condensation / 4.2: deprotection / 5.1: Iodination / 6.1: Substitution;
DOI:10.1016/S0040-4039(00)00710-3

Reference yield:

: 294844-18-1
(S)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-(toluene-4-sulfonylamino)-propionic acid methyl ester

: 295337-51-8
2-(4-{(R)-3-(6-Benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2-[[(E)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enyl]-(toluene-4-sulfonyl)-amino]-propoxy}-butyl)-malonic acid dimethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 3 h / 20 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 20 °C

3.1: 2,6-di-tert-butyl-pyridine; silver trifluoromethanesulfonate / dichloromethane / 4 h / 20 °C

3.2: DDQ / 22; 15 / 4 h / 20 °C

4.1: 1H-imidazole; iodine; triphenylphosphine / toluene; acetonitrile / 10 h / 20 °C

5.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide / 12 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; 2,6-di-tert-butyl-pyridine; iodine; silver trifluoromethanesulfonate; sodium hydride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile; 1.1: Mitsunobu reaction / 2.1: Reduction / 3.1: Condensation / 3.2: deprotection / 4.1: Iodination / 5.1: Substitution;
DOI:10.1016/S0040-4039(00)00710-3