N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide

Base Information

• Chemical Name: N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide
• CAS No.: 1066876-09-2
• Molecular Formula: C₂₂H₃₀N₂O₅S
• Molecular Weight: 434.557

Synonyms:N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide

Chemical Property of N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide

Chemical Property:

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Technology Process of N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide

There total 5 articles about N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide 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:

N-[(1S,2R)-1-benzyl-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][(R)-(tetrahydro-2-furanyl)methyl]amino]propyl]carbamic acid tert-butyl ester (919081-51-9) → N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide (1066876-09-2)

Guidance literature:

With trifluoroacetic acid; In dichloromethane; for 1h;

DOI:10.1021/jm060666p

Reference yield:

{1-benzyl-2-hydroxy-3-[(tetrahydro-furan-2-ylmethyl)-amino]-propyl}-carbamic acid tert-butyl ester (1066876-07-0) → N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide (1066876-09-2)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. Na₂CO₃ / CH₂Cl₂ / 20 °C

2: TFA / CH₂Cl₂ / 1 h

With sodium carbonate; trifluoroacetic acid; In dichloromethane;

DOI:10.1021/jm060666p

Reference yield:

m-Methoxybenzenesulfonyl chloride (10130-74-2) → N-(3-amino-2-hydroxy-4-phenyl-butyl)-4-methoxy-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide (1066876-09-2)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. Na₂CO₃ / CH₂Cl₂ / 20 °C

2: TFA / CH₂Cl₂ / 1 h

With sodium carbonate; trifluoroacetic acid; In dichloromethane;

DOI:10.1021/jm060666p

upstream raw materials:

N-[(1S,2R)-1-benzyl-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][(R)-(tetrahydro-2-furanyl)methyl]amino]propyl]carbamic acid tert-butyl ester

{1-benzyl-2-hydroxy-3-[(tetrahydro-furan-2-ylmethyl)-amino]-propyl}-carbamic acid tert-butyl ester

m-Methoxybenzenesulfonyl chloride

(1-oxiranyl-2-phenylethyl)carbamic acid tert-butyl ester

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