4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

Base Information

Chemical Name:4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine
CAS No.:173318-29-1
Molecular Formula:C₂₇H₃₄N₆O₄S₄
Molecular Weight:634.869
Hs Code.:

4-(dimethylamino)-2,6-bis<<N-<3-<(2-nitrophenyl)dithio>propyl>amino>methyl>pyridine

Synonyms:4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

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Chemical Property of 4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

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Technology Process of 4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

There total 4 articles about 4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine 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: 90.0%

: 173318-27-9
4-(dimethylamino)-2,6-bis<-N-<3-<(2-nitrophenyl)dithio>propyl>amino>methyl>pyridine

: 173318-29-1
4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

Guidance literature:: With hydrogenchloride; 3-Methylindole; In methanol; dichloromethane; for 9h; Ambient temperature;
DOI:10.1021/jm950831t

Reference yield:

: 7669-54-7
2-nitrobenzenesulfenyl chloride

: 173318-29-1
4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / acetic acid / 16 h / Ambient temperature

2: 90 percent / 3-methylindole, 0.5 N aq. HCl / CH₂Cl₂; methanol / 9 h / Ambient temperature

With hydrogenchloride; 3-Methylindole; acetic acid; In methanol; dichloromethane;
DOI:10.1021/jm950831t

Reference yield:

: 153504-00-8
4-(dimethylamino)pyridine-2,6-dicarbaldehyde

: 173318-29-1
4-(dimethylamino)-2,6-bis<propyl>amino>methyl>pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 39 percent / sodium cyanoborohydride / methanol / 36 h / Ambient temperature

2: 61 percent / acetic acid / 16 h / Ambient temperature

3: 90 percent / 3-methylindole, 0.5 N aq. HCl / CH₂Cl₂; methanol / 9 h / Ambient temperature

With hydrogenchloride; 3-Methylindole; sodium cyanoborohydride; acetic acid; In methanol; dichloromethane;
DOI:10.1021/jm950831t