(6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

Base Information

Chemical Name:(6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester
CAS No.:1332344-13-4
Molecular Formula:C₂₅H₂₆N₂O₃
Molecular Weight:402.493
Hs Code.:

Synonyms:(6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

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Chemical Property of (6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

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Technology Process of (6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

There total 10 articles about (6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl 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: 87.0%

: 100-52-7
benzaldehyde

: 104-94-9
4-methoxy-aniline

: 260967-14-4
benzyl N-[(1E)-prop-1-en-1-yl]-carbamate

: 1332344-13-4
(6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

Guidance literature:: benzaldehyde; 4-methoxy-aniline; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;

benzyl N-[(1E)-prop-1-en-1-yl]-carbamate; With (R)-2,6-bis-(4-chloro-phenyl)-4-oxo-3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-ol; In dichloromethane; at 0 ℃; for 17h; enantioselective reaction; Inert atmosphere;
DOI:10.1002/chir.23403

Reference yield: 33.0%

: 19064-76-7,94664-76-3
N-benzylidene-4-methoxyaniline oxide

: 1078123-69-9
benzyl (E/Z)-prop-1-enylcarbamate

: 1332344-13-4
(6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

Guidance literature:: With 4-hydroxy-2,6-diphenyl-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide; copper hydroxide; In methanol; dichloromethane; water; at 20 ℃; for 1h; stereoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/ejoc.201900547

Reference yield:

: 783-08-4
[4-(benzylideneamino)phenyl]methanol

: 260967-14-4
benzyl N-[(1E)-prop-1-en-1-yl]-carbamate

: 1332344-13-4
(6-methoxy-3-methyl-2-phenyl-1,2,3,4-tetrahydro-quinolin-4-yl)carbamic acid benzyl ester

Guidance literature:: With (R)-2,6-bis-(4-chloro-phenyl)-4-oxo-3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-ol; In dichloromethane; at 0 ℃; for 1h; optical yield given as %ee; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ja205891m