(S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

Base Information

Chemical Name:(S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide
CAS No.:1357194-10-5
Molecular Formula:C₁₈H₁₉ClN₆OS
Molecular Weight:402.907
Hs Code.:

Synonyms:(S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

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Chemical Property of (S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

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Technology Process of (S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

There total 4 articles about (S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide 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:

: 1357194-19-4
C₁₈H₁₇ClN₈OS

: 1357194-10-5
(S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; at 20 ℃; for 5h; Inert atmosphere;
DOI:10.1016/j.bmcl.2011.11.080

Reference yield:

: 1261080-60-7
methyl 2-(3-(dimethylamino)acryloyl) thiazole-5-carboxylate

: 1357194-10-5
(S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium ethanolate / ethanol / 16 h / 20 - 80 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 5 h / 20 °C

3: palladium 10% on activated carbon; hydrogen / 5 h / 20 °C / Inert atmosphere

With palladium 10% on activated carbon; hydrogen; sodium ethanolate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.11.080

Reference yield:

: 1261080-59-4
methyl 2-acetylthiazole-5-carboxylate

: 1357194-10-5
(S)-N-(1-amino-3-(4-chlorophenyl)propan-2-yl)-2-(2-(methylamino)pyrimidin-4-yl)thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: toluene / 15 h / Reflux

2: sodium ethanolate / ethanol / 16 h / 20 - 80 °C

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 5 h / 20 °C

4: palladium 10% on activated carbon; hydrogen / 5 h / 20 °C / Inert atmosphere

With palladium 10% on activated carbon; hydrogen; sodium ethanolate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmcl.2011.11.080