3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

Base Information

Chemical Name:3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
CAS No.:1048035-13-7
Molecular Formula:C₂₀H₂₆ClIN₄O₃S
Molecular Weight:564.875
Hs Code.:

Synonyms:3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

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Chemical Property of 3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

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Technology Process of 3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

There total 8 articles about 3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine 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:

: 110-91-8,99108-56-2
morpholine

: 1049806-97-4
C₁₆H₁₇ClIN₃O₃S

: 1048035-13-7
3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane;
DOI:10.1016/j.bmcl.2009.09.014

Reference yield:

: 42860-04-8
4-chloro-3-iodobenzoic acid

: 1048035-13-7
3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 3 - 17 h / 0 - 20 °C

2.1: triethylamine / dichloromethane / 14 h / 0 - 20 °C

2.2: 14 h / 0 - 20 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

3.2: 48 h

4.1: hydrogenchloride; water / acetone / 5 h / 55 °C

5.1: acetic acid / dichloromethane / 0.17 h

5.2: 60 h

With hydrogenchloride; oxalyl dichloride; water; caesium carbonate; acetic acid; triethylamine; N,N-dimethyl-formamide; In dichloromethane; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1049102-99-9
C₁₀H₁₈N₂O₃S

: 1048035-13-7
3-(4-Chloro-3-iodo-phenyl)-5-methanesulfonyl-1-(3-morpholin-4-yl-propyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 14 h / 0 - 20 °C

1.2: 14 h / 0 - 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

2.2: 48 h

3.1: hydrogenchloride; water / acetone / 5 h / 55 °C

4.1: acetic acid / dichloromethane / 0.17 h

4.2: 60 h

With hydrogenchloride; water; caesium carbonate; acetic acid; triethylamine; In dichloromethane; N,N-dimethyl-formamide; acetone;