ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate

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Chemical Name:ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate
CAS No.:92592-07-9
Molecular Formula:C₂₄H₂₁N₅O₁₁S
Molecular Weight:587.524
Hs Code.:

Synonyms:ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate

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Chemical Property of ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate

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Technology Process of ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate

There total 2 articles about ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate 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: 47.0%

: 4457-32-3
4-nitrobenzyl chloroformate

: 65052-66-6
2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid-S-ethyl ester

: 92592-06-8
ethyl (E)-α-methoxyimino-α-<2-(4-nitrobenzyloxycarbonylamino)thiazol-4-yl>acetate

: 92592-07-9
ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; for 2h;

Reference yield:

: 60845-87-6
ethyl γ-bromo-α-methoxyiminoacetoacetate

: 92592-07-9
ethyl (E)-α-methoxyimino-α-<3-(4-nitrobenzyloxycarbonyl)-2-(4-nitrobenzyloxycarbonylimino)-2,3-dihydrothiazol-4-yl>acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / 2.) sodium carbonate / 1.) EtOH, reflux, 2 h, 2.) ethyl acetate, H₂O

2: 47 percent / aq.sodium hydrogen carbonate / CH₂Cl₂ / 2 h

With sodium hydrogencarbonate; sodium carbonate; In dichloromethane;