[3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

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Chemical Name:[3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester
CAS No.:80090-31-9
Molecular Formula:C₃₂H₃₇N₃O₉
Molecular Weight:607.66
Hs Code.:

Synonyms:[3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

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Chemical Property of [3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

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Technology Process of [3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

There total 9 articles about [3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-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: 65.0%

: 80090-29-5
8-carboethoxymethoxy-5-<3-(N-benzyloxycarbonyl-3,4-dimethoxyphenethylamino)-2-hydroxypropoxy>-3,4-dihydrocarbostyril

: 80090-31-9
[3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

Guidance literature:: With ammonium hydroxide;
DOI:10.1248/cpb.29.2166

Reference yield:

: 59430-56-7
5,8-Dihydroxy-3,4-dihydro-2(1H)-quinolinone

: 80090-31-9
[3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 48 percent / K₂CO₃ / acetone; H₂O / 4 h / Heating

2: 56 percent / K₂CO₃ / propan-2-ol / 5 h / 70 - 80 °C

3: 43.6 percent / methanol / 20 h / Ambient temperature

4: 77.2 percent / hydrogen / 10percent Pd-C / methanol; H₂O / 8 h / Ambient temperature

5: 96 percent / 10percent Na₂CO₃, NaOH / acetone; H₂O / 1.5 h / Ambient temperature

6: 100 percent / 2N NaOH / methanol / Ambient temperature

7: 73.8 percent / K₂CO₃ / acetone; H₂O / 9 h / Ambient temperature

8: 65 percent / 28percent NH₄OH

With ammonium hydroxide; sodium hydroxide; hydrogen; sodium carbonate; potassium carbonate; palladium on activated charcoal; In methanol; water; isopropyl alcohol; acetone;
DOI:10.1248/cpb.29.2166

Reference yield:

: 59826-16-3
8-(Benzyloxy)-5-hydroxy-3,4-dihydro-2(1H)-quinolinone

: 80090-31-9
[3-(8-Carbamoylmethoxy-2-oxo-1,2,3,4-tetrahydro-quinolin-5-yloxy)-2-hydroxy-propyl]-[2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 56 percent / K₂CO₃ / propan-2-ol / 5 h / 70 - 80 °C

2: 43.6 percent / methanol / 20 h / Ambient temperature

3: 77.2 percent / hydrogen / 10percent Pd-C / methanol; H₂O / 8 h / Ambient temperature

4: 96 percent / 10percent Na₂CO₃, NaOH / acetone; H₂O / 1.5 h / Ambient temperature

5: 100 percent / 2N NaOH / methanol / Ambient temperature

6: 73.8 percent / K₂CO₃ / acetone; H₂O / 9 h / Ambient temperature

7: 65 percent / 28percent NH₄OH

With ammonium hydroxide; sodium hydroxide; hydrogen; sodium carbonate; potassium carbonate; palladium on activated charcoal; In methanol; water; isopropyl alcohol; acetone;
DOI:10.1248/cpb.29.2166