(+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:(+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:1064203-04-8
Molecular Formula:C₂₁H₂₈N₂O₇S
Molecular Weight:452.529
Hs Code.:

Synonyms:(+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

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Technology Process of (+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

There total 6 articles about (+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-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: 95.0%

: 1064202-99-8
(+/-)-6-hydroxy-7-methoxy-1-methyl-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

: 1064203-04-8
(+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With sulphamoyl chloride; In N,N-dimethyl acetamide; toluene; at 20 ℃; for 96h; Inert atmosphere;
DOI:10.1002/cmdc.201300412

Reference yield: 95.0%

: 1064203-04-8
(+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:

Reference yield:

: 55161-43-8
N-{2-[3-(benzyloxy)-4-methoxyphenyl]ethyl}acetamide

: 1064203-04-8
(+/-)-7-methoxy-1-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate / toluene / 3 h / 140 °C

2: sodium tetrahydroborate / ethanol / 1.5 h / 0 °C

3: triethylamine / ethanol / 0.5 h / 170 °C / Microwave irradiation

4: palladium 10% on activated carbon; hydrogen / ethanol; tetrahydrofuran / 18 h / 20 °C

5: sulphamoyl chloride / toluene; N,N-dimethyl acetamide / 96 h / 20 °C / Inert atmosphere

With sodium tetrahydroborate; palladium 10% on activated carbon; sulphamoyl chloride; hydrogen; triethylamine; trichlorophosphate; In tetrahydrofuran; ethanol; N,N-dimethyl acetamide; toluene;
DOI:10.1002/cmdc.201300412