methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

Base Information

Chemical Name:methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate
CAS No.:436843-87-7
Molecular Formula:C₂₀H₁₉BrN₂O₅S
Molecular Weight:479.351
Hs Code.:

Synonyms:methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

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Chemical Property of methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

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Technology Process of methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

There total 1 articles about methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]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: 90.0%

: 101085-25-0
5-bromo-4-(bromomethyl)-2-phenyl-1,3-oxazole

: 59724-68-4
N-phenylsulfonyl-L-alanine methyl ester

: 436843-87-7
methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

Guidance literature:: With potassium carbonate; In acetonitrile; for 2h; Heating;
DOI:10.1021/jo010665z

Reference yield: 74.0%

: 436843-87-7
methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

: 221454-91-7
(6S)-6-methyl-2-phenyl-5-(phenylsulfonyl)-5,6-dihydro[1,3]oxazolo[4,5-c]pyridin-7(4H)-one

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; at -100 ℃;
DOI:10.1021/jo010665z

Reference yield:

: 436843-87-7
methyl (2S)-2-[[(5-bromo-2-phenyl-1,3-oxazol-4-yl)methyl](phenylsulfonyl)amino]propanoate

: N-[(3S,4S,5R,6S)-4-hydroxy-5-methoxy-6-methyl-1-(phenylsulfonyl)piperidinyl]-N-methylbenzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: 74 percent / n-BuLi / hexane; tetrahydrofuran / -100 °C

2.1: 93 percent / NaBH₄ / tetrahydrofuran; ethanol / 2 h / 20 °C

3.1: NaH / tetrahydrofuran / 0.5 h / 20 °C

3.2: 97 percent / tetrahydrofuran / 2 h

4.1: 86 percent / CH₂Cl₂ / 0 °C

5.1: 63 percent / aq. KOH / CH₂Cl₂

6.1: 75 percent / NaBH₄ / methanol / 3 h / 20 °C

With potassium hydroxide; sodium tetrahydroborate; n-butyllithium; sodium hydride; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane;
DOI:10.1021/jo010665z