3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

Base Information

Chemical Name:3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one
CAS No.:132119-42-7
Molecular Formula:C₁₄H₁₅N₅O₂S
Molecular Weight:317.371
Hs Code.:

Synonyms:3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

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Chemical Property of 3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

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Technology Process of 3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

There total 6 articles about 3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one 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: 81.0%

: 132119-41-6
1-(2-Benzyloxy-ethylsulfanylmethyl)-5-imino-2,5-dihydro-1H-[1,2,3]triazole-4-carboxylic acid amide

: 109-94-4
formic acid ethyl ester

: 132119-42-7
3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

Guidance literature:: With sodium ethanolate; In ethanol; for 14h; Heating;

Reference yield:

: 622-08-2,1201808-31-2
2-Benzyloxyethanol

: 132119-42-7
3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / pyridine, Zeolite A-3 / 3 h / 0 °C

2: 1.) thiourea, 2.) aq. NaOH / 1.) ethanol, reflux, 24 h, 2.) reflux, 18 h

3: 1,2-dichloro-ethane / 1.5 h / 0 °C

4: NaN₃ / acetonitrile / 2 h / Heating

5: 61 percent / aq. KOH / dimethylformamide / 15 h / 0 °C

6: 81 percent / EtONa / ethanol / 14 h / Heating

With pyridine; potassium hydroxide; sodium hydroxide; sodium azide; Zeolite A-3; sodium ethanolate; thiourea; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 4981-83-3
2-(Benzyloxy)ethyl p-toluenesulfonate

: 132119-42-7
3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) thiourea, 2.) aq. NaOH / 1.) ethanol, reflux, 24 h, 2.) reflux, 18 h

2: 1,2-dichloro-ethane / 1.5 h / 0 °C

3: NaN₃ / acetonitrile / 2 h / Heating

4: 61 percent / aq. KOH / dimethylformamide / 15 h / 0 °C

5: 81 percent / EtONa / ethanol / 14 h / Heating

With potassium hydroxide; sodium hydroxide; sodium azide; sodium ethanolate; thiourea; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;