2,6-bis<-N-tosylamino>methyl>pyridine

Base Information

Chemical Name:2,6-bis<-N-tosylamino>methyl>pyridine
CAS No.:125682-94-2
Molecular Formula:C₃₁H₄₃N₃O₁₂S₄
Molecular Weight:777.959
Hs Code.:

2,6-bis<<N-<5-(mesyloxy)-3-oxapentyl>-N-tosylamino>methyl>pyridine

Synonyms:2,6-bis<-N-tosylamino>methyl>pyridine

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Chemical Property of 2,6-bis<-N-tosylamino>methyl>pyridine

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Technology Process of 2,6-bis<-N-tosylamino>methyl>pyridine

There total 4 articles about 2,6-bis<-N-tosylamino>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: 98.0%

: 124-63-0
methanesulfonyl chloride

: 125682-93-1
2,6-bis<methyl>pyridine

: 125682-94-2
2,6-bis<-N-tosylamino>methyl>pyridine

Guidance literature:: With triethylamine; In dichloromethane; for 3h; Ambient temperature;
DOI:10.1002/hlca.19890720525

Reference yield:

: 34984-16-2
2,6-bis(aminomethyl)pyridine

: 125682-94-2
2,6-bis<-N-tosylamino>methyl>pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent

2: 72 percent / K₂CO₃ / dimethylformamide / 1.) 85 deg C, 24h, 2.) room temp., 24h

3: 98 percent / Et₃N / CH₂Cl₂ / 3 h / Ambient temperature

With potassium carbonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19890720525

Reference yield:

: 112633-27-9
2,6-bis<(p-tosylamino)methyl>pyridine

: 125682-94-2
2,6-bis<-N-tosylamino>methyl>pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / K₂CO₃ / dimethylformamide / 1.) 85 deg C, 24h, 2.) room temp., 24h

2: 98 percent / Et₃N / CH₂Cl₂ / 3 h / Ambient temperature

With potassium carbonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19890720525