(S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:(S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:80656-78-6
Molecular Formula:C₂₀H₂₅NO₅
Molecular Weight:359.422
Hs Code.:

Synonyms:(S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Suppliers and Price of (S)-7-hydroxy-6-methoxy-1-(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 (S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of (S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

There total 4 articles about (S)-7-hydroxy-6-methoxy-1-(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:

: 80601-90-7
(S)-N-benzyloxycarbonyl-7-benzyloxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

: 80656-78-6
(S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In ethanol; for 1h; under 760 Torr; Ambient temperature;
DOI:10.1248/cpb.29.2816

Reference yield:

: 30418-38-3
(-)-Trimetoquinol

: 80656-78-6
(S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / NaHCO₃ / CHCl₃; H₂O / 1 h / 5 °C / then 2 h room temperature

2: 25 percent / K₂CO₃ / dimethylsulfoxide / 18 h / Ambient temperature

3: 99 percent / K₂CO₃ / dimethylsulfoxide / 48 h / Ambient temperature

4: 11 mg / hydrogen, 10percent aq. HCl / 10percent Pd-C / ethanol / 1 h / 760 Torr / Ambient temperature

With hydrogenchloride; hydrogen; sodium hydrogencarbonate; potassium carbonate; palladium on activated charcoal; In ethanol; chloroform; water; dimethyl sulfoxide;
DOI:10.1248/cpb.29.2816

Reference yield:

: 80601-87-2
(S)-N-benzyloxycarbonyl-7-benzyloxy-6-hydroxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

: 80656-78-6
(S)-7-hydroxy-6-methoxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / K₂CO₃ / dimethylsulfoxide / 48 h / Ambient temperature

2: 11 mg / hydrogen, 10percent aq. HCl / 10percent Pd-C / ethanol / 1 h / 760 Torr / Ambient temperature

With hydrogenchloride; hydrogen; potassium carbonate; palladium on activated charcoal; In ethanol; dimethyl sulfoxide;
DOI:10.1248/cpb.29.2816