7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

Base Information

Chemical Name:7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine
CAS No.:442909-23-1
Molecular Formula:C₁₆H₁₅N₇O
Molecular Weight:321.341
Hs Code.:

Synonyms:7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

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Chemical Property of 7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

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Technology Process of 7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

There total 5 articles about 7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine 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:

: 442910-11-4
C₂₁H₂₃N₇O₃

: 442909-23-1
7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 2h;
DOI:10.1021/jm800961g

Reference yield:

: 172353-84-3
tert-butyl((4-hydroxymethyl)phenyl)(methyl)carbamate

: 442909-23-1
7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: carbon tetrabromide; triphenylphosphine / dichloromethane / 1 h / 0 °C

2.1: sodium hydride / tetrahydrofuran / 0 °C

2.2: 16 h / 20 °C

3.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

With hydrogenchloride; carbon tetrabromide; sodium hydride; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1021/jm800961g

Reference yield:

: 10541-83-0,937737-33-2
N-methyl-p-aminobenzoic acid

: 442909-23-1
7-(2-furyl)-3-(4-(N-methylamino)benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 48 h / Reflux

2.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 1 h / 0 °C

2.2: 1 h / -78 - 20 °C

3.1: carbon tetrabromide; triphenylphosphine / dichloromethane / 1 h / 0 °C

4.1: sodium hydride / tetrahydrofuran / 0 °C

4.2: 16 h / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; carbon tetrabromide; sodium hydride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1021/jm800961g