(+)-α-(<(1S,2R,4R,R_S)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide

Base Information

• Chemical Name: (+)-α-(<(1S,2R,4R,R_S)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide
• CAS No.: 155834-23-4
• Molecular Formula: C₂₂H₂₇NO₅S
• Molecular Weight: 417.526

Synonyms:(+)-α-(<(1S,2R,4R,R_S)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide

Chemical Property of (+)-α-(<(1S,2R,4R,R_S)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide

Chemical Property:

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Technology Process of (+)-α-(<(1S,2R,4R,R_S)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide

There total 4 articles about (+)-α-(<(1S,2R,4R,R_S)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide 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: 100.0%

(-)-α-(<(1S,2R,4R)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylthio)-N-(4-methoxybenzyl)maleimide (155834-33-6) → (+)-α-(<(1S,2R,4R,RS)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide (155834-23-4)

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; Ambient temperature;

Reference yield:

(1S,2R,4R)-(-)-10-mercaptoisoboneol (71242-58-5) → (+)-α-(<(1S,2R,4R,RS)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide (155834-23-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 99 percent / Et₃N / CH₂Cl₂ / 25 °C

2: 93 percent / N-chlorosuccinimide / CCl₄ / Heating

3: 100 percent / m-chloroperbenzoic acid / CH₂Cl₂ / Ambient temperature

With N-chloro-succinimide; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrachloromethane; dichloromethane;

Reference yield:

1-((4-methoxyphenyl)methyl)-1H-pyrrole-2,5-dione (140480-96-2) → (+)-α-(<(1S,2R,4R,RS)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylsulfinyl)-N-(4-methoxybenzyl)maleimide (155834-23-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 99 percent / Et₃N / CH₂Cl₂ / 25 °C

2: 93 percent / N-chlorosuccinimide / CCl₄ / Heating

3: 100 percent / m-chloroperbenzoic acid / CH₂Cl₂ / Ambient temperature

With N-chloro-succinimide; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrachloromethane; dichloromethane;

upstream raw materials:

(-)-α-(<(1S,2R,4R)-2-hydroxy-7,7-dimethylbicyclo<2.2.1>heptan-1-yl>methylthio)-N-(4-methoxybenzyl)maleimide

(1S,2R,4R)-(-)-10-mercaptoisoboneol

1-((4-methoxyphenyl)methyl)-1H-pyrrole-2,5-dione

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