7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Base Information

Chemical Name:7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline
CAS No.:892405-27-5
Molecular Formula:C₂₅H₃₃FN₂O₃S
Molecular Weight:460.613
Hs Code.:

Synonyms:7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

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Chemical Property of 7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

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Technology Process of 7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

There total 9 articles about 7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline 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:

: 892405-32-2
methanesulfonic acid 3-[4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinolin-7-yloxy]-propyl ester

: 78197-27-0
4-fluoropiperidine

: 892405-27-5
7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: With sodium carbonate; potassium iodide; In butan-1-ol; for 18h; Heating;
DOI:10.1016/j.bmcl.2006.11.036

Reference yield:

: 245510-06-9
3-(3-hydroxy-propoxy)-benzaldehyde

: 892405-27-5
7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 7 steps

1: 100 percent / methanol; H₂O / 0 °C

2: 100 percent / NaBH₄ / methanol; H₂O / 18.5 h / 0 - 23 °C

3: (i-Pr)2NEt / tetrahydrofuran / 0.75 h / 23 °C

4: methanesulfonic acid / 18 h / 60 °C

5: NaCNBH₃ / methanol / 0.08 h / 23 °C

6: Et₃N / CH₂Cl₂ / 0.33 h / 0 - 23 °C

7: Na₂CO₃; KI / butan-1-ol / 18 h / Heating

With sodium tetrahydroborate; methanesulfonic acid; sodium cyanoborohydride; sodium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; methanol; dichloromethane; water; butan-1-ol;
DOI:10.1016/j.bmcl.2006.11.036

Reference yield:

: 3-{3-[(E)-Methyliminomethyl]-phenoxy}-propan-1-ol

: 892405-27-5
7-[3-(4-fluoro-piperidin-1-yl)-propoxy]-4-(4-methanesulfonyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 6 steps

1: 100 percent / NaBH₄ / methanol; H₂O / 18.5 h / 0 - 23 °C

2: (i-Pr)2NEt / tetrahydrofuran / 0.75 h / 23 °C

3: methanesulfonic acid / 18 h / 60 °C

4: NaCNBH₃ / methanol / 0.08 h / 23 °C

5: Et₃N / CH₂Cl₂ / 0.33 h / 0 - 23 °C

6: Na₂CO₃; KI / butan-1-ol / 18 h / Heating

With sodium tetrahydroborate; methanesulfonic acid; sodium cyanoborohydride; sodium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; methanol; dichloromethane; water; butan-1-ol;
DOI:10.1016/j.bmcl.2006.11.036