2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline
CAS No.:1064205-46-4
Molecular Formula:C₂₆H₂₈ClNO₃
Molecular Weight:437.966
Hs Code.:

Synonyms:2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of 2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

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Technology Process of 2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

There total 7 articles about 2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-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: 77.0%

: 1064202-11-4
(+/-)-6-benzyloxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline

: 3771-13-9
2-(bromomethyl)-1-chloro-4-methoxybenzene

: 1064205-46-4
2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80 ℃; for 20h;

Reference yield:

: 321125-47-7
(+/-)-2-benzyloxy-1-methoxy-4-(2-nitropropyl)benzene

: 1064205-46-4
2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 5 steps

1: hydrazine / nickel / methanol; water / 19 h / 0 - 40 °C

2: triethylamine / 24 h / 0 - 20 °C

3: formaldehyd; toluene-4-sulfonic acid / toluene / Heating / reflux

4: sodium hydroxide; water / ethanol / 44 h / Heating / reflux

5: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 h / 80 °C

With sodium hydroxide; formaldehyd; water; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; hydrazine; nickel; In methanol; ethanol; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1064202-02-3
2-benzyloxy-1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene

: 1064205-46-4
2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 6 steps

1: sodium tetrahydroborate / tetrahydrofuran; ethanol / 1.83 h / 0 - 20 °C

2: hydrazine / nickel / methanol; water / 19 h / 0 - 40 °C

3: triethylamine / 24 h / 0 - 20 °C

4: formaldehyd; toluene-4-sulfonic acid / toluene / Heating / reflux

5: sodium hydroxide; water / ethanol / 44 h / Heating / reflux

6: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 h / 80 °C

With sodium hydroxide; sodium tetrahydroborate; formaldehyd; water; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; hydrazine; nickel; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;