2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

Base Information

Chemical Name:2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate
CAS No.:1367367-33-6
Molecular Formula:C₁₉H₁₈N₈O₄S₂
Molecular Weight:486.535
Hs Code.:

Synonyms:2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

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Chemical Property of 2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

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Technology Process of 2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

There total 7 articles about 2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate 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: 68.0%

: 1367367-32-5
5-amino-3-(2-hydroxyethyl)-1-methyl-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-2-one

: 98-59-9
p-toluenesulfonyl chloride

: 1367367-33-6
2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: With pyridine; at 25 - 27 ℃;
DOI:10.1021/acsmedchemlett.7b00175

Reference yield:

: 1367366-94-6
2-amino-6-hydrazino-9-(2-hydroxyethyl)-7-methylpurin-8-one

: 1367367-33-6
2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: benzotriazol-1-ol; 4-methyl-morpholine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 3 h / 25 - 27 °C

2: N,O-bis-(trimethylsilyl)-acetamide; 1,1,1,3,3,3-hexamethyl-disilazane / 14 h / 140 - 150 °C

3: pyridine / 25 - 27 °C

With 4-methyl-morpholine; pyridine; N,O-bis-(trimethylsilyl)-acetamide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1,1,1,3,3,3-hexamethyl-disilazane; In N,N-dimethyl-formamide;
DOI:10.1021/acsmedchemlett.7b00175

Reference yield:

: 2-[(2,5-diamino-6-chloro-pyrimidin-4-yl)amino]ethanol

: 1367367-33-6
2-(5-amino-1-methyl-2-oxo-8-thiazol-2-yl-[1,2,4]triazolo[5,1-i]purin-3-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / acetonitrile / 24 h / 0 - 27 °C

2: potassium carbonate / acetonitrile / 16 h / 20 - 60 °C

3: hydrazine hydrate / ethanol / 16 h / 100 - 110 °C

4: benzotriazol-1-ol; 4-methyl-morpholine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 3 h / 25 - 27 °C

5: N,O-bis-(trimethylsilyl)-acetamide; 1,1,1,3,3,3-hexamethyl-disilazane / 14 h / 140 - 150 °C

6: pyridine / 25 - 27 °C

With 4-methyl-morpholine; pyridine; N,O-bis-(trimethylsilyl)-acetamide; potassium carbonate; benzotriazol-1-ol; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1,1,1,3,3,3-hexamethyl-disilazane; In ethanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/acsmedchemlett.7b00175