N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

Base Information

Chemical Name:N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt
CAS No.:1235330-55-8
Molecular Formula:C₂₃H₂₀ClN₃O₄S₃*H₃N
Molecular Weight:551.111
Hs Code.:

Synonyms:N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

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Chemical Property of N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

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Technology Process of N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

There total 6 articles about N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt 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:

: C₂₃H₂₀ClN₃OS₂

: 1235330-55-8
N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

Guidance literature:: C₂₃H₂₀ClN₃OS₂; With pyridine-SO₃ complex; In pyridine; at 20 ℃; for 0.0833333h;

With ammonium hydroxide; In pyridine; water;

Reference yield:

: 1000394-52-4
2-(3-chlorophenyl)-N-{(S)-2-(4-nitrophenyl)-1-[2-(thiophen-2-yl)thiazol-4-yl]ethyl}acetamide

: 1235330-55-8
N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / methanol / 18 h

2: pyridine; sulfur trioxide pyridine complex / 0.08 h / 20 °C

With pyridine; hydrogen; sulfur trioxide pyridine complex; palladium 10% on activated carbon; In methanol;

Reference yield:

: 127106-74-5
(S)-[3-diazo-1-(4-nitrobenzyl)-2-oxo-propyl]carbamic acid tert-butyl ester

: 1235330-55-8
N-{4-[(2S)-2-[2-(3-chlorophenyl)acetamido]-2-[2-(thiophen-2-yl)-1,3-thiazol-4-yl]ethyl]phenyl}sulfamic acid ammonium salt

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen bromide / water; tetrahydrofuran / 1.5 h / 0 °C

2: acetonitrile / 5 h / Reflux

3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 0 - 20 °C

4: hydrogen / palladium 10% on activated carbon / methanol / 18 h

5: pyridine; sulfur trioxide pyridine complex / 0.08 h / 20 °C

With pyridine; hydrogen bromide; hydrogen; sulfur trioxide pyridine complex; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile;