N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

Base Information

Chemical Name:N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine
CAS No.:952338-67-9
Molecular Formula:C₂₀H₂₇IN₂O₅SSi
Molecular Weight:562.501
Hs Code.:

Synonyms:N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

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Chemical Property of N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

Chemical Property:

Purity/Quality:

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Technology Process of N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

There total 7 articles about N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine 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:

: 1057340-19-8
tert-butyl N-[2-(benzyloxy)-4-iodophenyl]-N-{{(tert-butoxycarbonyl)[2-(trimethylsilyl)ethyl]amino}sulfonyl}glycinate

: 952338-67-9
N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 27783-55-7
5-iodo-2-nitrophenol

: 952338-67-9
N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 65 °C

2: iron; acetic acid / ethanol / 1.5 h / 100 °C

3: potassium carbonate / N,N-dimethyl-formamide / 4 h / 50 °C

4: triethylamine / dichloromethane / 0.5 h / 0 °C

5: di-isopropyl azodicarboxylate; triphenylphosphine / toluene / 19 h

6: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With di-isopropyl azodicarboxylate; iron; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; trifluoroacetic acid; In ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1057340-17-6
2-benzyloxy-4-iodo-1-nitrobenzene

: 952338-67-9
N-[2-(benzyloxy)-4-iodophenyl]-N-({[2-(trimethylsilyl)ethyl]amino}sulfonyl)glycine

Guidance literature:: Multi-step reaction with 5 steps

1: iron; acetic acid / ethanol / 1.5 h / 100 °C

2: potassium carbonate / N,N-dimethyl-formamide / 4 h / 50 °C

3: triethylamine / dichloromethane / 0.5 h / 0 °C

4: di-isopropyl azodicarboxylate; triphenylphosphine / toluene / 19 h

5: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With di-isopropyl azodicarboxylate; iron; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; trifluoroacetic acid; In ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;