(S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

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Chemical Name:(S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one
CAS No.:790698-15-6
Molecular Formula:C₃₇H₅₁NO₇Si
Molecular Weight:649.9
Hs Code.:

Synonyms:(S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

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Chemical Property of (S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

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Technology Process of (S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

There total 3 articles about (S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one 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:

: 2930-05-4,14618-80-5,89616-40-0,16495-13-9
(S)-benzyl glycidyl ether

: 790698-15-6
(S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: 99 percent / n-BuLi / tetrahydrofuran / -10 - 25 °C

2.1: NaH / tetrahydrofuran / 1 h / 0 °C

2.2: 98 percent / tetrahydrofuran / 0 - 20 °C

3.1: Et₃N; pivaloyl chloride / diethyl ether / 1 h / 0 °C

3.2: 78 percent / n-BuLi / tetrahydrofuran; hexane; diethyl ether / 2 h / 0 °C

4.1: 91 percent / 4-(dimethylamino)-pyridine; DIEA / CH₂Cl₂ / 72 h / 20 °C

With dmap; n-butyllithium; pivaloyl chloride; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ja0455852

Reference yield:

: 748770-49-2
4-(S)-benzyl-3-{2-[1-(S)-benzyloxymethyl-allyloxy]acetyl}oxazolidin-2-one

: 790698-15-6
(S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / 4-(dimethylamino)-pyridine; DIEA / CH₂Cl₂ / 72 h / 20 °C

With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/ja0455852

Reference yield:

: 790698-14-5
((S)-1-Benzyloxymethyl-allyloxy)-acetic acid

: 790698-15-6
(S)-4-Benzyl-3-[(2R,3S)-2-((S)-1-benzyloxymethyl-allyloxy)-3-methoxymethoxy-5-triisopropylsilanyl-pent-4-ynoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: Et₃N; pivaloyl chloride / diethyl ether / 1 h / 0 °C

1.2: 78 percent / n-BuLi / tetrahydrofuran; hexane; diethyl ether / 2 h / 0 °C

2.1: 91 percent / 4-(dimethylamino)-pyridine; DIEA / CH₂Cl₂ / 72 h / 20 °C

With dmap; pivaloyl chloride; triethylamine; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane;
DOI:10.1021/ja0455852