7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Base Information

Chemical Name:7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
CAS No.:188576-50-3
Molecular Formula:C₃₁H₃₅NO₆
Molecular Weight:517.622
Hs Code.:

Synonyms:7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

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Chemical Property of 7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

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Technology Process of 7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

There total 8 articles about 7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl 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: 98.0%

: 109394-53-8
(4-(benzyloxy)phenyl)chloroacetic acid ethyl ester

: 188576-49-0
7-hydroxy-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid tert-butyl ester

: 188576-50-3
7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Guidance literature:: With potassium carbonate; In acetonitrile; for 24h; Heating;
DOI:10.1021/jm9800402

Reference yield:

: 7651-83-4
isoquinolin-7-ol

: 188576-50-3
7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / H₂, glacial AcOH / PtO₂ / 48 h / Ambient temperature

2: 89 percent / Et₃N / CH₂Cl₂ / 1 h / 5 °C

3: 98 percent / K₂CO₃ / acetonitrile / 24 h / Heating

With hydrogen; potassium carbonate; acetic acid; triethylamine; platinum(IV) oxide; In dichloromethane; acetonitrile;
DOI:10.1021/jm9800402

Reference yield:

: 1700-37-4
3-Benzyloxybenzaldehyde

: 188576-50-3
7-<(4-(benzyloxy)phenyl)(ethoxycarbonyl)methoxy>-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: toluene / 6 h / Heating

2: trifluoroacetic acid anhydride, BF₃*Et₂O / toluene / 120 h / Ambient temperature

3: 83 percent / H₂, glacial AcOH / PtO₂ / 48 h / Ambient temperature

4: 89 percent / Et₃N / CH₂Cl₂ / 1 h / 5 °C

5: 98 percent / K₂CO₃ / acetonitrile / 24 h / Heating

With boron trifluoride diethyl etherate; hydrogen; potassium carbonate; acetic acid; triethylamine; trifluoroacetic anhydride; platinum(IV) oxide; In dichloromethane; toluene; acetonitrile;
DOI:10.1021/jm9800402