2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

Base Information

Chemical Name:2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate
CAS No.:910864-41-4
Molecular Formula:C₄₉H₆₁O₁₁PSi
Molecular Weight:885.076
Hs Code.:

Synonyms:2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

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Chemical Property of 2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

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Technology Process of 2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

There total 8 articles about 2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate 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: 49.0%

: 910864-29-8
2-O-benzyl-4,6-di-O-p-methoxybenzyl-1,5-di-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

: Phosphoric acid dibenzyl ester (1S,2S,3S,4S,5R,6S)-2-benzyloxy-3,5-dihydroxy-4,6-bis-(4-methoxy-benzyloxy)-cyclohexyl ester

: 910864-41-4
2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

Guidance literature:: With acetyl chloride; In methanol; at 0 ℃; for 12h;
DOI:10.1021/jo0610816

Reference yield:

: 2-O-benzyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol-1,3,5-O-orthoformate

: 910864-41-4
2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

Guidance literature:: Multi-step reaction with 5 steps

1: 55 percent / aq. HCl / methanol / 18 h / 20 °C

2: 53 percent / Et₃N / BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe / toluene

3: 90 percent / imidazole / dimethylformamide / 48 h / 50 °C

4: 88 percent / NaH / tetrahydrofuran / 1 h / 20 °C

5: 49 percent / AcCl / methanol / 12 h / 0 °C

With 1H-imidazole; hydrogenchloride; sodium hydride; triethylamine; acetyl chloride; BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo0610816

Reference yield:

: 910864-22-1
2-O-benzyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol

: 910864-41-4
2-O-benzyl-4,6-di-O-p-methoxybenzyl-1-O-tert-butyldimethylsilyl-D-myo-inositol-3-dibenzyl phosphate

Guidance literature:: Multi-step reaction with 4 steps

1: 53 percent / Et₃N / BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe / toluene

2: 90 percent / imidazole / dimethylformamide / 48 h / 50 °C

3: 88 percent / NaH / tetrahydrofuran / 1 h / 20 °C

4: 49 percent / AcCl / methanol / 12 h / 0 °C

With 1H-imidazole; sodium hydride; triethylamine; acetyl chloride; BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo0610816