2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline

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Chemical Name:2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline
CAS No.:1417155-83-9
Molecular Formula:C₄₆H₃₇N₃O₃
Molecular Weight:679.818
Hs Code.:

Synonyms:2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of 2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline

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Technology Process of 2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline

There total 2 articles about 2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-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: 75.0%

: 1417155-77-1
N-benzyl-N-(2-bromo-4,5-dimethoxybenzyl)-1-(1,3-diphenyl-1H-pyrazol-4-yl)-3-(2-phenoxyphenyl)prop-2-yn-1-amine

: 1417155-83-9
2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With palladium diacetate; potassium carbonate; triphenylphosphine; In N,N-dimethyl-formamide; at 100 ℃; for 2h; Inert atmosphere;
DOI:10.1021/ol303326g

Reference yield:

: 512197-88-5
1-ethynyl-2-phenoxybenzene

: 21487-45-6
1,3-diphenyl-4-formylpyrazole

: 89525-53-1
1-bromo-2-benzylaminomethyl-4,5-dimethoxybenzene

: 1417155-83-9
2-benzyl-3-(1,3-diphenyl-1H-pyrazol-4-yl)-6,7-dimethoxy-4-(9Hxanthen-9-ylidene)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide / toluene / 3 h / 100 °C

2: palladium diacetate; triphenylphosphine; potassium carbonate / N,N-dimethyl-formamide / 2 h / 100 °C / Inert atmosphere

With copper(l) iodide; palladium diacetate; potassium carbonate; triphenylphosphine; In N,N-dimethyl-formamide; toluene;
DOI:10.1021/ol303326g