2S,3R,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid

Base Information

Chemical Name:2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid
CAS No.:125488-23-5
Molecular Formula:C₃₃H₃₄N₄O₂
Molecular Weight:518.659
Hs Code.:

Synonyms:2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid

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Technology Process of 2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid

There total 3 articles about 2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid 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:

: 1631-28-3,25989-85-9
N-p-tolylphenylmaleimide

: 125488-23-5
2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid

Guidance literature:: Multi-step reaction with 2 steps

1: CDCl₃ / -60 °C

2: CHCl₃ / 3 h / Ambient temperature

In chloroform-d1; chloroform;

Reference yield:

: 111335-61-6
2-tert-Butyl-3-methoxy-4-methyl-2,4-dihydropyrrolo<3,4-b>indol

: 125488-23-5
2S*,3R*,4S*-1-Benzylimino-4-t-butylamino-9-methyl-1,2,3,4-tetrahydrocarbazol-2,3-dicarbonsaeure-N-(4-methylphenyl)imid

Guidance literature:: Multi-step reaction with 2 steps

1: CDCl₃ / -60 °C

2: CHCl₃ / 3 h / Ambient temperature

In chloroform-d1; chloroform;