(S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Base Information

Chemical Name:(S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline
CAS No.:1263210-10-1
Molecular Formula:C₂₆H₂₉NO₄
Molecular Weight:419.521
Hs Code.:

Synonyms:(S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Suppliers and Price of (S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

There total 7 articles about (S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline 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: 81.0%

: 1263210-03-2
2-[4,5-dihydro-4-((R)-1-methylethyl)-2-oxazolyl]-(S)-1-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydroisoquinoline

: 1263210-10-1
(S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: With toluene-4-sulfonic acid; hydrazine hydrate; In ethanol; for 6h; Inert atmosphere; Reflux;
DOI:10.3998/ark.5550190.0012.514

Reference yield:

: 1263210-09-8
7-(benzyloxy)-2-[(4R)-4,5-dihydro-4-(1-methylethyl)-2-oxazolyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline

: 1263210-10-1
(S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1.1: tert.-butyl lithium / tetrahydrofuran; pentane / 5.5 h / -78 °C / Inert atmosphere

1.2: 0.5 h / -100 °C

2.1: toluene-4-sulfonic acid; hydrazine hydrate / ethanol / 6 h / Inert atmosphere; Reflux

With tert.-butyl lithium; toluene-4-sulfonic acid; hydrazine hydrate; In tetrahydrofuran; ethanol; pentane;
DOI:10.3998/ark.5550190.0012.514

Reference yield:

: 63909-38-6,1860-56-6
3-methoxy-4-benzyloxy-ω-nitrostyrolene

: 1263210-10-1
(S)-l-(4-methoxymethoxybenzyl)-6-methoxy-7-benzyloxy-1,2,3,4-tetrahydro-isoquinoline

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 10 °C / Inert atmosphere; Reflux

2.1: 12 h / Inert atmosphere; Reflux

3.1: phosphorus pentachloride / chloroform; N,N-dimethyl-formamide / -78 - 20 °C / Inert atmosphere

4.1: sodium tetrahydroborate / ethanol / 15 - 20 °C / Inert atmosphere

5.1: toluene-4-sulfonic acid / benzene / Inert atmosphere; Reflux

6.1: tert.-butyl lithium / tetrahydrofuran; pentane / 5.5 h / -78 °C / Inert atmosphere

6.2: 0.5 h / -100 °C

7.1: toluene-4-sulfonic acid; hydrazine hydrate / ethanol / 6 h / Inert atmosphere; Reflux

With sodium tetrahydroborate; lithium aluminium tetrahydride; phosphorus pentachloride; tert.-butyl lithium; toluene-4-sulfonic acid; hydrazine hydrate; In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide; pentane; benzene;
DOI:10.3998/ark.5550190.0012.514