(R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

Base Information

Chemical Name:(R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate
CAS No.:1061742-43-5
Molecular Formula:C₃₁H₃₁N₃O₇S
Molecular Weight:589.669
Hs Code.:

Synonyms:(R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

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Chemical Property of (R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

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Technology Process of (R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

There total 8 articles about (R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate 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: 53.0%

: 1061742-73-1
C₃₇H₄₅N₃O₇SSi

: 1061742-43-5
(R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 5h;

Reference yield:

: 1061742-69-5
tert-butyl (2R)-4-[(benzyloxy)carbonylamino]-2-[1,1'-(biphenyl-4-yl-sulfonyl)-(benzyloxy)amino]butanoate

: 1061742-43-5
(R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid / dichloromethane / 5 h / 0 °C

2.1: dichloromethane / 0 °C

2.2: 20 h / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 5 h / 0 °C

With trifluoroacetic acid; In dichloromethane;

Reference yield:

: 1061742-72-0
C₃₁H₃₀N₂O₇S

: 1061742-43-5
(R)-benzyl 3-(N-(benzyloxy)biphenyl-4-ylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloromethane / 0 °C

1.2: 20 h / 20 °C

2.1: trifluoroacetic acid / dichloromethane / 5 h / 0 °C

With trifluoroacetic acid; In dichloromethane;