(1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

Base Information

Chemical Name:(1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one
CAS No.:129958-89-0
Molecular Formula:C₂₉H₄₁NO₅
Molecular Weight:483.648
Hs Code.:

Synonyms:(1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

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Chemical Property of (1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

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Technology Process of (1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

There total 4 articles about (1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-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: 59.1%

: 123279-29-8,123355-78-2
(1S,4R)-1-<1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-oxo-2-phenyl-1-ethyl)-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

: 129958-89-0
(1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

: 123355-81-7
(1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-phenyl-1-ethyl)-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

: 123279-32-3
(1S,4R)-1-<(1S)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-phenyl-1-ethyl)-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

Guidance literature:: With hydrogen; 10% palladium on active carbon; In acetic acid; trifluoroacetic acid; for 24h; under 2250.2 Torr; Ambient temperature;
DOI:10.1002/ardp.19903230605

Reference yield:

: 123355-81-7
(1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-phenyl-1-ethyl)-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

: 129958-89-0
(1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

Guidance literature:: With hydrogen; platinum(IV) oxide; In hydrogenchloride; methanol;
DOI:10.1002/ardp.19903230605

Reference yield:

: 123279-30-1,123355-79-3
(1S,4R)-1-<1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(4-Chlorophenyl)-2-oxo-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

: 129958-89-0
(1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C (10percent Pd) / acetic acid; trifluoroacetic acid / 44 h / 2250.2 Torr / Ambient temperature

2: H₂ / PtO₂ / methanol; HCl

With hydrogen; platinum(IV) oxide; 10% palladium on active carbon; In hydrogenchloride; methanol; acetic acid; trifluoroacetic acid;
DOI:10.1002/ardp.19903230605