methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

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Chemical Name:methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate
CAS No.:923579-15-1
Molecular Formula:C₂₆H₃₉N₃O₇SSi
Molecular Weight:565.763
Hs Code.:

Synonyms:methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

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Chemical Property of methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

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Technology Process of methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

There total 4 articles about methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate 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: 50.0%

: 175717-73-4
(R)-1-((tert-butyldimethylsilyl)oxy)propan-2-amine

: 923578-97-6
(2R)-2-benzyl-2-methoxycarbonyl-1-(2-nitrobenzenesulfonyl)-aziridine

: 923579-15-1
methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

Guidance literature:: In acetonitrile; at 20 ℃; for 20h;
DOI:10.1021/ol0626241

Reference yield:

: 923578-94-3
methyl (R)-2-amino-2-benzyl-3-hydroxypropanoate

: 923579-15-1
methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / KHCO₃ / acetonitrile / 16 h / Heating

2: 50 percent / acetonitrile / 20 h / 20 °C

With potassium hydrogencarbonate; In acetonitrile;
DOI:10.1021/ol0626241

Reference yield:

: (2S,4R)-4-benzyl-2-(tert-butyl)-3-formyl-4-methoxycarbonyl-1,3-oxazolidine

: 923579-15-1
methyl (R)-2-benzyl-3-[(R)-2-(tert-butyldimethylsilyloxy)-1-methyl-ethylamino]-2-(2-nitrobenzenesulfonylamino)-propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / HCl / methanol; H₂O / 7 h / Heating

2: 89 percent / KHCO₃ / acetonitrile / 16 h / Heating

3: 50 percent / acetonitrile / 20 h / 20 °C

With hydrogenchloride; potassium hydrogencarbonate; In methanol; water; acetonitrile;
DOI:10.1021/ol0626241