{1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

Base Information

Chemical Name:{1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester
CAS No.:345235-03-2
Molecular Formula:C₄₅H₄₈N₄O₃
Molecular Weight:692.901
Hs Code.:

Synonyms:{1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

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Chemical Property of {1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

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Technology Process of {1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

There total 6 articles about {1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester 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:

: 513-35-9
2-methyl-but-2-ene

: 17430-98-7
[(1S)-1-cyclohexylethyl]amine

: 433981-16-9
3-[4-(9H-Fluoren-9-ylmethoxycarbonylamino)-piperidin-1-ylmethyl]-2-phenyl-quinoline-4-carboxylic Acid

: 345235-03-2
{1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

Guidance literature:: With sodium hydroxide; triethylamine; In tetrahydrofuran; dichloromethane; water; ethyl acetate;

Reference yield:

: 43071-45-0
3-methyl-2-phenylquinoline-4-carboxylic acid

: 345235-03-2
{1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: oxalyl chloride / CH₂Cl₂ / 0.5 h / 20 °C

1.2: DMF / CH₂Cl₂ / 0.5 h

2.1: CH₂Cl₂ / 18 h

3.1: 70 percent / NBS; dibenzoylperoxide / acetonitrile / 28 h / Heating

4.1: iPr₂NEt / tetrahydrofuran / 50 °C

5.1: aq. HCl / 4 h / Heating

6.1: HBTU; TEA / tetrahydrofuran; CH₂Cl₂ / 18 h / Heating

With hydrogenchloride; N-Bromosuccinimide; oxalyl dichloride; TEA; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; dibenzoyl peroxide; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm000501v

Reference yield:

: 174636-71-6
3-methyl-2-phenylquinoline-4-carbonyl chloride

: 345235-03-2
{1-[4-((S)-1-Cyclohexyl-ethylcarbamoyl)-2-phenyl-quinolin-3-ylmethyl]-piperidin-4-yl}-carbamic Acid 9H-fluoren-9-ylmethyl Ester

Guidance literature:: Multi-step reaction with 5 steps

1: CH₂Cl₂ / 18 h

2: 70 percent / NBS; dibenzoylperoxide / acetonitrile / 28 h / Heating

3: iPr₂NEt / tetrahydrofuran / 50 °C

4: aq. HCl / 4 h / Heating

5: HBTU; TEA / tetrahydrofuran; CH₂Cl₂ / 18 h / Heating

With hydrogenchloride; N-Bromosuccinimide; TEA; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; dibenzoyl peroxide; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm000501v