2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

• Chemical Name: 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline
• CAS No.: 1615201-22-3
• Molecular Formula: C₂₄H₂₂N₄O₃S
• Molecular Weight: 446.53
• Mol file: 1615201-22-3.mol

Synonyms:2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline

Chemical Property of 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline

There total 5 articles about 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline 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: 84.0%

1-phenoxy-2-propyne (13610-02-1) + 2-((4-azidophenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline (1615201-43-8) → 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline (1615201-22-3)

Guidance literature:

With copper(ll) sulfate pentahydrate; Vitamin C; In water; tert-butyl alcohol; at 20 ℃;

DOI:10.1016/j.ejmech.2014.05.019

Reference yield:

N-(4-nitrobenzenesulfonyl)-2-phenylethylamine (52374-24-0) → 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline (1615201-22-3)

Guidance literature:

Multi-step reaction with 4 steps

1.1: formic acid / 2 h / 20 °C / Reflux

2.1: tin(II) chloride dihdyrate / ethanol / 4 h / Reflux

3.1: hydrogenchloride; sodium nitrite / ethanol; water / 0.25 h

3.2: 0.5 h / 20 °C

4.1: copper(ll) sulfate pentahydrate; Vitamin C / water; tert-butyl alcohol / 20 °C

With hydrogenchloride; copper(ll) sulfate pentahydrate; tin(II) chloride dihdyrate; Vitamin C; sodium nitrite; In formic acid; ethanol; water; tert-butyl alcohol; 1.1: |Pictet-Spengler Synthesis;

DOI:10.1016/j.ejmech.2014.05.019

Reference yield:

2-((4-nitrophenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline (64880-92-8) → 2-((4-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)phenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline (1615201-22-3)

Guidance literature:

Multi-step reaction with 3 steps

1.1: tin(II) chloride dihdyrate / ethanol / 4 h / Reflux

2.1: hydrogenchloride; sodium nitrite / ethanol; water / 0.25 h

2.2: 0.5 h / 20 °C

3.1: copper(ll) sulfate pentahydrate; Vitamin C / water; tert-butyl alcohol / 20 °C

With hydrogenchloride; copper(ll) sulfate pentahydrate; tin(II) chloride dihdyrate; Vitamin C; sodium nitrite; In ethanol; water; tert-butyl alcohol;

DOI:10.1016/j.ejmech.2014.05.019

upstream raw materials:

N-(4-nitrobenzenesulfonyl)-2-phenylethylamine

2-((4-nitrophenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline

2-((4-aminophenyl)sulfonyl)-1,2,3,4-tetrahydroisoquinoline

1-phenoxy-2-propyne