ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

Base Information

Chemical Name:ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide
CAS No.:1616070-43-9
Molecular Formula:C₂₂H₂₄N₄O₆S
Molecular Weight:472.522
Hs Code.:

Synonyms:ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

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Chemical Property of ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

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Technology Process of ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

There total 6 articles about ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide 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:

: 64-17-5
ethanol

: 1269523-38-7
3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbonitrile 1,1-dioxide

: 1616070-43-9
ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

Guidance literature:: With acetyl chloride; at 0 - 25 ℃;

Reference yield:

: 1228773-89-4
(R)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetic acid

: 1616070-43-9
ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride; 1H-imidazole / dichloromethane / 0.5 h / -40 - 20 °C

1.2: 0 - 25 °C

2.1: ammonium hydroxide / 48 h / Inert atmosphere; Reflux

3.1: acetyl chloride / 0 - 25 °C

With 1H-imidazole; ammonium hydroxide; thionyl chloride; acetyl chloride; In dichloromethane;

Reference yield:

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

: 1616070-43-9
ethyl 3-((S)-hydroxy((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)methyl)-4H-benzo[e][1,2,4]thiadiazine-7-carbimidate 1,1-dioxide

Guidance literature:: Multi-step reaction with 5 steps

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

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

3.1: thionyl chloride; 1H-imidazole / dichloromethane / 0.5 h / -40 - 20 °C

3.2: 0 - 25 °C

4.1: ammonium hydroxide / 48 h / Inert atmosphere; Reflux

5.1: acetyl chloride / 0 - 25 °C

With 1H-imidazole; ammonium hydroxide; potassium phosphate; copper(l) iodide; thionyl chloride; acetyl chloride; cis-N,N'-dimethyl-1,2-diaminocyclohexane; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;