methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

Base Information

Chemical Name:methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate
CAS No.:1620012-99-8
Molecular Formula:C₁₇H₁₈F₂N₂O₅S
Molecular Weight:400.403
Hs Code.:

Synonyms:methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

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Chemical Property of methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

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Technology Process of methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

There total 3 articles about methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate 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: 39.0%

: 870779-02-5
(2,6-difluoro-3-methoxyphenyl)boronic acid

: 1620011-00-8
methyl 2-bromo-5-[(tert-butoxycarbonyl)amino]-1,3-thiazole-4-carboxylate

: 1620012-99-8
methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

Guidance literature:: With potassium phosphate; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)); water; In 1,4-dioxane; at 20 - 40 ℃; for 16h; Inert atmosphere;

Reference yield:

: 1239464-24-4
methyl 5-amino-1,3-thiazole-4-carboxylate

: 1620012-99-8
methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / tetrahydrofuran / 1 h / 20 - 30 °C

2: dmap; triethylamine / tetrahydrofuran / 16 h / 20 - 30 °C

3: water; potassium phosphate; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)) / 1,4-dioxane / 16 h / 20 - 40 °C / Inert atmosphere

With dmap; potassium phosphate; N-Bromosuccinimide; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)); water; triethylamine; In tetrahydrofuran; 1,4-dioxane;

Reference yield:

: 1373223-08-5
methyl 5-amino-2-bromo-1,3-thiazole-4-carboxylate

: 1620012-99-8
methyl 5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazole-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; triethylamine / tetrahydrofuran / 16 h / 20 - 30 °C

2: water; potassium phosphate; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)) / 1,4-dioxane / 16 h / 20 - 40 °C / Inert atmosphere

With dmap; potassium phosphate; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)); water; triethylamine; In tetrahydrofuran; 1,4-dioxane;