(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

Base Information

Chemical Name:(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide
CAS No.:92472-59-8
Molecular Formula:C₂₉H₄₂N₂O₂
Molecular Weight:450.665
Hs Code.:

Synonyms:(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

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Chemical Property of (4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

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Technology Process of (4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

There total 8 articles about (4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide 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:

: 302-97-6
androst-4-en-3-one-17β-carboxylic acid

: 92472-59-8
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) pyridine, oxalyl chloride / 1.) toluene, RT, 1 h, 2.) toluene, 0.5 h

2: 87 percent / Na₂CO₃, NaIO₄, KMnO₄ / 2-methyl-propan-2-ol; H₂O / Heating

3: ethanol / 8 h / 180 °C

4: H₂ / PtO₂ / acetic acid / 3 h / 25 - 60 °C / 2327.2 Torr

With pyridine; potassium permanganate; sodium periodate; oxalyl dichloride; hydrogen; sodium carbonate; platinum(IV) oxide; In ethanol; water; acetic acid; tert-butyl alcohol;
DOI:10.1021/jm00378a028

Reference yield:

: 92472-48-5
(4aR,4bS,6aS,7S,9aS,9bS)-4a,6a-Dimethyl-2-oxo-1-phenyl-2,3,4,4a,4b,5,6,6a,7,8,9,9a,9b,10-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

: 92472-59-8
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

Guidance literature:: With hydrogen; platinum(IV) oxide; In acetic acid; at 25 - 60 ℃; for 3h; under 2327.2 Torr;
DOI:10.1021/jm00378a028

Reference yield:

: 145-13-1
Pregnenolone

: 92472-59-8
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-1-phenyl-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic acid diethylamide

Guidance literature:: Multi-step reaction with 8 steps

1: I₂ / 1 h / Heating

2: methanol / 1 h / Heating

3: 1.) Al(i-PrO)3, 2.) Supercel, Darco KB / 1.) toluene, cyclohexanone, reflux, 1 h, 2.) toluene, cyclohexanone, water, 15 min

4: 1.71 kg / 10percent KOH / methanol / Heating

5: 1.) pyridine, oxalyl chloride / 1.) toluene, RT, 1 h, 2.) toluene, 0.5 h

6: 87 percent / Na₂CO₃, NaIO₄, KMnO₄ / 2-methyl-propan-2-ol; H₂O / Heating

7: ethanol / 8 h / 180 °C

8: H₂ / PtO₂ / acetic acid / 3 h / 25 - 60 °C / 2327.2 Torr

With pyridine; potassium hydroxide; potassium permanganate; sodium periodate; oxalyl dichloride; hydrogen; iodine; silica gel; aluminum isopropoxide; sodium carbonate; pyrographite; platinum(IV) oxide; In methanol; ethanol; water; acetic acid; tert-butyl alcohol;
DOI:10.1021/jm00378a028