3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

Base Information

Chemical Name:3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide
CAS No.:1354718-73-2
Molecular Formula:C₂₄H₂₃N₅O₃S
Molecular Weight:461.544
Hs Code.:

Synonyms:3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

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Chemical Property of 3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

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Technology Process of 3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

There total 6 articles about 3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide 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:

: C₂₀H₁₆N₄O₃

: 17899-48-8
2-amino-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

: 1354718-73-2
3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

Guidance literature:: In N,N-dimethyl acetamide; at 100 ℃; for 72h;

Reference yield:

: 19438-10-9
methyl 3-hydroxybenzoate

: 1354718-73-2
3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 19 h / 0 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 0 - 20 °C

3.1: pyridine; trichlorophosphate / 1 h / 0 °C

4.1: sodium hydroxide; water / methanol / 1 h / 50 °C

4.2: 20 °C / pH ~ 5

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / 1 h / 20 °C

6.1: N,N-dimethyl acetamide / 72 h / 100 °C

With pyridine; water; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; diethylazodicarboxylate; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl acetamide;

Reference yield:

: 113429-82-6
3-((S)-1-carboxy-ethoxy)-benzoic acid methyl ester

: 1354718-73-2
3-[(S)-1-(4-cyano-phenylcarbamoyl)-ethoxy]-N-(5-methyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-yl)-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine; trichlorophosphate / 1 h / 0 °C

2.1: sodium hydroxide; water / methanol / 1 h / 50 °C

2.2: 20 °C / pH ~ 5

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / 1 h / 20 °C

4.1: N,N-dimethyl acetamide / 72 h / 100 °C

With pyridine; water; N-ethyl-N,N-diisopropylamine; sodium hydroxide; trichlorophosphate; In methanol; N,N-dimethyl acetamide;