2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

Base Information

Chemical Name:2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide
CAS No.:1616068-86-0
Molecular Formula:C₂₀H₂₁N₅O₃
Molecular Weight:379.418
Hs Code.:

Synonyms:2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

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Chemical Property of 2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

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Technology Process of 2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

There total 7 articles about 2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide 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:

: 1616070-42-8
ethyl 2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carbimidate

: 1616068-86-0
2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

Guidance literature:: With ammonia; In methanol; at 25 ℃;

Reference yield:

: 1228774-07-9
(R)-tert-butyl 2-hydroxy-2-((R)-3-oxomorpholin-2-yl)acetate

: 1616068-86-0
2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

Guidance literature:: Multi-step reaction with 6 steps

1: copper(l) iodide; potassium phosphate; cis-N,N'-dimethyl-1,2-diaminocyclohexane / N,N-dimethyl-formamide / 4 h / 110 °C / Inert atmosphere

2: trifluoroacetic acid / dichloromethane / 1 h / 25 °C

3: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 25 °C

4: acetic acid / 0.33 h / 120 °C / Microwave irradiation

5: acetyl chloride / 48 h / 0 - 25 °C

6: ammonia / methanol / 25 °C

With potassium phosphate; copper(l) iodide; ammonia; acetic acid; N-ethyl-N,N-diisopropylamine; acetyl chloride; cis-N,N'-dimethyl-1,2-diaminocyclohexane; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1228773-88-3
(R)-tert-butyl 2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetate

: 1616068-86-0
2-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-1H-benzo[d]imidazole-6-carboximidamide

Guidance literature:: Multi-step reaction with 5 steps

1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C

2: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 25 °C

3: acetic acid / 0.33 h / 120 °C / Microwave irradiation

4: acetyl chloride / 48 h / 0 - 25 °C

5: ammonia / methanol / 25 °C

With ammonia; acetic acid; N-ethyl-N,N-diisopropylamine; acetyl chloride; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; dichloromethane; N,N-dimethyl-formamide;