(S_P,4'S_C)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide

Base Information

• Chemical Name: (S_P,4'S_C)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide
• CAS No.: 1270965-86-0
• Molecular Formula: C₁₈H₁₆N₃O₄P
• Molecular Weight: 369.316

Synonyms:(S_P,4'S_C)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide

Chemical Property of (S_P,4'S_C)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide

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Technology Process of (S_P,4'S_C)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide

There total 3 articles about (S_P,4'S_C)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide 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:

(S)-4-benzyl-2-(N-cyanimino)oxazolidine (1270965-73-5) + 2-chloro-4H-benzo[d][1,3,2]dioxaphosphinine 2-oxide (127164-51-6) → (SP,4'SC)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide (1270965-86-0) + (RP,4'SC)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide (1270965-80-4)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 7h;

DOI:10.1002/chem.201002657

Reference yield:

L-Phenylalaninol (3182-95-4) → (SP,4'SC)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide (1270965-86-0) + (RP,4'SC)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide (1270965-80-4)

Guidance literature:

Multi-step reaction with 2 steps

1: methanol / 18 h / 20 - 65 °C

2: triethylamine / dichloromethane / 7 h / 20 °C

With triethylamine; In methanol; dichloromethane;

DOI:10.1002/chem.201002657

Reference yield:

salicylic alcohol (90-01-7) → (SP,4'SC)-2-(4'-benzyl-2'-N-cyanimino-oxazolidin-3'-yl)-4H-1,3,2-benzodioxaphosphorin-2-oxide (1270965-86-0)

Guidance literature:

Multi-step reaction with 2 steps

1: triethylamine; trichlorophosphate / tetrahydrofuran / 6 h / -70 - 20 °C

2: triethylamine / dichloromethane / 20 °C

With triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jm3008085

upstream raw materials:

(S)-4-benzyl-2-(N-cyanimino)oxazolidine

2-chloro-4H-benzo[d][1,3,2]dioxaphosphinine 2-oxide

L-Phenylalaninol

salicylic alcohol

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