Technology Process of (3R,4R)-(-)-4-fluoro-6-methyl-3-propyl-1,2,3,4-tetrahydroisoquinoline
There total 6 articles about (3R,4R)-(-)-4-fluoro-6-methyl-3-propyl-1,2,3,4-tetrahydroisoquinoline which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
bis(1,5-cyclooctadiene)diiridium(I) dichloride; trichloroisocyanuric acid; hydrogen; (R)-segphos;
In
1,4-dioxane; isopropyl alcohol;
at 30 ℃;
for 20h;
under 31029.7 Torr;
enantioselective reaction;
Autoclave;
DOI:10.1021/acs.orglett.7b02502
- Guidance literature:
-
With
bis(1,5-cyclooctadiene)diiridium(I) dichloride; 1,3-dichloro-5,5-dimethylhydantoin; hydrogen; (+)-(R)-[2,3,2',3'-tetrahydro-5,5'-bi(1,4-benzodioxin)-6,6'-diyl]bis(diphenylphosphane);
In
1,4-dioxane; isopropyl alcohol;
at 30 ℃;
for 20h;
under 30003 Torr;
enantioselective reaction;
DOI:10.1039/c3cc45341c
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 20 °C
2: lithium carbonate; silver nitrate; N-fluorobis(benzenesulfon)imide / N,N-dimethyl acetamide / 20 °C
3: hydrogenchloride / diethyl ether / 0.01 h / 20 °C
4: hydrogen; bis(1,5-cyclooctadiene)diiridium(I) dichloride; (+)-(R)-[2,3,2',3'-tetrahydro-5,5'-bi(1,4-benzodioxin)-6,6'-diyl]bis(diphenylphosphane); 1,3-dichloro-5,5-dimethylhydantoin / 1,4-dioxane; isopropyl alcohol / 20 h / 30 °C / 30003 Torr
With
hydrogenchloride; bis(1,5-cyclooctadiene)diiridium(I) dichloride; 1,3-dichloro-5,5-dimethylhydantoin; hydrogen; lithium carbonate; silver nitrate; N-fluorobis(benzenesulfon)imide; (+)-(R)-[2,3,2',3'-tetrahydro-5,5'-bi(1,4-benzodioxin)-6,6'-diyl]bis(diphenylphosphane);
In
1,4-dioxane; diethyl ether; N,N-dimethyl acetamide; isopropyl alcohol;
DOI:10.1039/c3cc45341c