(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

Base Information

Chemical Name:(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid
CAS No.:135996-20-2
Molecular Formula:C₃₈H₃₅N₃O₇S₂
Molecular Weight:709.844
Hs Code.:

Synonyms:(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

Suppliers and Price of (Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

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Chemical Property of (Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

Chemical Property:

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Technology Process of (Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

There total 8 articles about (Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid 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:

: 68363-44-0
2-oxo-2-(2-(tritylamino)thiazol-4-yl)acetic acid

: 135996-19-9
tert-butyl 2-aminooxy-2-(4-acetoxyphenylthio)acetate

: 135996-20-2
(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

Guidance literature:: In methanol; for 1h; Ambient temperature;
DOI:10.7164/antibiotics.47.477

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 135996-20-2
(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

Guidance literature:: Multi-step reaction with 6 steps

2: pyridine / CH₂Cl₂

3: N-chlorosuccinimide / CCl₄

4: 1.) triethylamine, 2.) pyridine

5: methylhydrazine

6: methanol / 1 h / Ambient temperature

With pyridine; N-chloro-succinimide; triethylamine; methylhydrazine; In methanol; tetrachloromethane; dichloromethane;
DOI:10.7164/antibiotics.47.477

Reference yield:

: 637-89-8
4-sulfanylphenol

: 135996-20-2
(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(tert-butoxycarbonyl)(4-acetoxyphenylthio)methoxy]imino]acetic acid

Guidance literature:: Multi-step reaction with 6 steps

2: pyridine / CH₂Cl₂

3: N-chlorosuccinimide / CCl₄

4: 1.) triethylamine, 2.) pyridine

5: methylhydrazine

6: methanol / 1 h / Ambient temperature

With pyridine; N-chloro-succinimide; triethylamine; methylhydrazine; In methanol; tetrachloromethane; dichloromethane;
DOI:10.7164/antibiotics.47.477