2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

Base Information

Chemical Name:2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one
CAS No.:350249-78-4
Molecular Formula:C₃₀H₃₀N₂O₄
Molecular Weight:482.579
Hs Code.:

Synonyms:2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

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Chemical Property of 2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

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Technology Process of 2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

There total 8 articles about 2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one 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:

: 350249-76-2
ethyl 2-{[N((S)-1-hydroxy-3-phenyl)prop-2-yl]-3-aminopropyl}-6-methoxy-7-benzyloxyquinoline-3-carboxylate

: 350249-78-4
2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

Guidance literature:: With sodium; In ethanol; for 24h; Heating;
DOI:10.1016/S0040-4020(01)00166-1

Reference yield:

: 2426-84-8
4-(benzyloxy)-5-methoxy-2-nitrobenzaldehyde

: 350249-78-4
2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

Guidance literature:: Multi-step reaction with 7 steps

1: 84 percent / ethanol / 2 h / Heating

2: 98 percent / sodium sulfide nonahydrate / ethanol / Heating

3: 77 percent / piperidine / ethanol / 24 h / Heating

4: formic acid / 2 h / 20 °C

5: ethanol / 0.75 h / 20 °C

6: sodium borohydride / ethanol / 0.75 h / 20 °C

7: 695 mg / sodium / ethanol / 24 h / Heating

With piperidine; sodium sulfide; sodium tetrahydroborate; formic acid; sodium; In ethanol; 2: Zinin reduction / 3: Friedlander condensation;
DOI:10.1016/S0040-4020(01)00166-1

Reference yield:

: 350249-67-1
ethyl-6,6-diethoxy-3-oxohexanoic acid

: 350249-78-4
2-[(S)-1-hydroxy-3-phenylprop-2-yl]-2,3,4,5-tetrahydro-8-benzyloxy-9-methoxyazepino[4,3-b]quinolin-1-one

Guidance literature:: Multi-step reaction with 5 steps

1: 77 percent / piperidine / ethanol / 24 h / Heating

2: formic acid / 2 h / 20 °C

3: ethanol / 0.75 h / 20 °C

4: sodium borohydride / ethanol / 0.75 h / 20 °C

5: 695 mg / sodium / ethanol / 24 h / Heating

With piperidine; sodium tetrahydroborate; formic acid; sodium; In ethanol; 1: Friedlander condensation;
DOI:10.1016/S0040-4020(01)00166-1