N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

Base Information

Chemical Name:N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide
CAS No.:74606-97-6
Molecular Formula:C₂₅H₂₀N₂O₃
Molecular Weight:396.445
Hs Code.:

Synonyms:N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

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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 N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

Chemical Property:

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Technology Process of N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

There total 6 articles about N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide 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:

: 98-88-4
benzoyl chloride

: 74606-97-6
N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) H₂, HCl / 1.) 10percent Pd/C / 1.) H₂O, 30 psi, 16 h

2: 1.) Ac₂O; 2.) AlCl₃ / 1.) 100 deg C, 15 min; 2.) dichloroethane, reflux, 30 min

With hydrogenchloride; aluminium trichloride; hydrogen; acetic anhydride; palladium on activated charcoal;
DOI:10.1021/ja00318a044

Reference yield:

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

: 74606-97-6
N-((2aS,4R)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) H₂, HCl / 1.) 10percent Pd/C / 1.) H₂O, 30 psi, 16 h

2: 1.) Ac₂O; 2.) AlCl₃ / 1.) 100 deg C, 15 min; 2.) dichloroethane, reflux, 30 min

With hydrogenchloride; aluminium trichloride; hydrogen; acetic anhydride; palladium on activated charcoal;
DOI:10.1021/ja00318a044

Reference yield:

: 74606-98-7,88636-10-6,88636-11-7,88668-83-1,88668-84-2
(S)-2-Benzoylamino-3-(1-benzoyl-2,3-dihydro-1H-indol-3-yl)-propionic acid

: 74606-97-6,74644-93-2,88668-85-3
N-((S)-1-Benzoyl-5-oxo-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-4-yl)-benzamide

Guidance literature:: With aluminium trichloride; acetic anhydride; Multistep reaction; 1.) 100 deg C, 15 min, 2.) ClCH₂-ClCH₂, reflux, 30 min;
DOI:10.1021/ja00536a067