S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

Base Information

Chemical Name:S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride
CAS No.:1254196-70-7
Molecular Formula:C₁₈H₂₀N₄O₂S*ClH
Molecular Weight:392.909
Hs Code.:

Synonyms:S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

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Chemical Property of S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

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Technology Process of S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

There total 7 articles about S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride 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:

: C₂₃H₂₈N₄O₄S

: 1254196-70-7
S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 22 ℃; for 16h;

Reference yield:

: 1213190-97-6
(S)-3-amino-3-(3-nitro-phenyl)-butyric acid methyl ester

: 1254196-70-7
S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 22 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 2 h / 22 °C / 760.05 Torr

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 22 °C

4: hydrogenchloride / 1,4-dioxane; methanol / 16 h / 22 °C

With hydrogenchloride; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; HATU; palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1254199-40-0
(S)-3-((R)-2-methyl-propane-2-sulfinylamino)-3-(3-nitro-phenyl)-butyric acid methyl ester

: 1254196-70-7
S-methyl-thiophene-1-carboxylic acid [3-((S)-2-amino-1,4-dimethyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-4-yl)phenyl]amide hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h / 22 °C

1.2: pH ~ 10

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 22 °C

3.1: hydrogen / palladium 10% on activated carbon / ethanol / 2 h / 22 °C / 760.05 Torr

4.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 22 °C

5.1: hydrogenchloride / 1,4-dioxane; methanol / 16 h / 22 °C

With hydrogenchloride; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; HATU; palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide;