4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

Base Information

Chemical Name:4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline
CAS No.:102781-13-5
Molecular Formula:C₃₁H₂₈F₃N₃O₅
Molecular Weight:579.576
Hs Code.:

4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-<m-(trifluoromethyl)phenoxy>quinoline

Synonyms:4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

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Chemical Property of 4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

Chemical Property:

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Technology Process of 4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

There total 4 articles about 4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline 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:

: 63460-47-9
2-(4-iodopentyl)-1,3-isoindolinedione

: [8-Amino-6-methoxy-5-(3-trifluoromethyl-phenoxy)-quinolin-4-yl]-methanol

: 102781-13-5
4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 90 ℃; Yield given;
DOI:10.1021/jm00149a004

Reference yield:

: 82333-37-7
6-methoxy-4-methyl-8-nitro-5-<3-(trifluoromethyl)phenoxy>quinoline

: 102781-13-5
4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / acetic acid, selenium dioxide / dioxane; acetic anhydride / Heating

2: 88 percent / sodium borohydride / tetrahydrofuran; ethanol / 1 h

3: 2N hydrochloric acid, stannous chloride, tin / tetrahydrofuran; ethanol / 1 h / 5 - 10 °C

4: triethylamine / dimethylformamide / 90 °C

With hydrogenchloride; tin; sodium tetrahydroborate; selenium(IV) oxide; acetic acid; triethylamine; tin(ll) chloride; In tetrahydrofuran; 1,4-dioxane; ethanol; acetic anhydride; N,N-dimethyl-formamide;
DOI:10.1021/jm00149a004

Reference yield:

: 98509-96-7
6-methoxy-8-nitro-5-quinoline-4-carboxaldehyde

: 102781-13-5
4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / sodium borohydride / tetrahydrofuran; ethanol / 1 h

2: 2N hydrochloric acid, stannous chloride, tin / tetrahydrofuran; ethanol / 1 h / 5 - 10 °C

3: triethylamine / dimethylformamide / 90 °C

With hydrogenchloride; tin; sodium tetrahydroborate; triethylamine; tin(ll) chloride; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00149a004