6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin

Base Information

Chemical Name:6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin
CAS No.:82841-85-8
Molecular Formula:C₂₇H₃₆N₂O₄
Molecular Weight:452.594
Hs Code.:

6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzo<de,g>chinolin

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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 6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin

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Technology Process of 6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin

There total 3 articles about 6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin 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:

: 82841-83-6
10-Amino-3,4-dihydro-6,7-dimethoxy-9-methylphenanthren-1(2H)-on

: 82841-85-8
6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / CHCl₃ / 3 h / Heating

2: 1.) diisopropylamine/n-butyllithium / 1.) THF, n-Hexane, 30 min, 0 deg C; 2.) from -78 deg C to room temp, 12 h

With n-butyllithium; diisopropylamine; In chloroform;
DOI:10.1002/jlac.198219820707

Reference yield:

: 82841-82-5
2,3,3a,6,7,11b-Hexahydro-9,10-dimethoxy-11b-methyl-2-thioxophenanthro<9,10-d>oxazol-4(5H)-on

: 82841-85-8
6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / 0.1 N HCl / acetone / 2.5 h / Heating

2: 59 percent / CHCl₃ / 3 h / Heating

3: 1.) diisopropylamine/n-butyllithium / 1.) THF, n-Hexane, 30 min, 0 deg C; 2.) from -78 deg C to room temp, 12 h

With hydrogenchloride; n-butyllithium; diisopropylamine; In chloroform; acetone;
DOI:10.1002/jlac.198219820707

Reference yield:

: 113832-57-8,1193-93-7
N-ethylidenecyclohexylamine

: 82841-84-7
10-Acetylamino-3,4-dihydro-6,7-dimethoxy-9-methylphenanthren-1(2H)-on

: 82841-85-8
6-Acetyl-5-cyclohexylamino-2,3,3a,4,5,6-hexahydro-3a-hydroxy-9,10-dimethoxy-7-methyl-1H-dibenzochinolin

Guidance literature:: With n-butyllithium; diisopropylamine; Yield given. Multistep reaction; 1.) THF, n-Hexane, 30 min, 0 deg C; 2.) from -78 deg C to room temp, 12 h;
DOI:10.1002/jlac.198219820707