3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

Base Information

Chemical Name:3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one
CAS No.:90521-21-4
Molecular Formula:C₁₄H₁₅ClN₆O₄S
Molecular Weight:398.83
Hs Code.:

3-(2-chloroethyl)-8-<N-(4-methoxybenzyl)sulfamoyl>imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

Synonyms:3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

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Technology Process of 3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

There total 4 articles about 3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-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: 42.0%

: 1943-83-5
2-chloroethyl isothiocyanate

: 90521-52-1
4-diazo-N-(4-methoxybenzyl)-4H-imidazole-5-sulfonamide

: 90521-21-4
3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

Guidance literature:: In ethyl acetate; for 48h; Ambient temperature;
DOI:10.1021/jm00385a018

Reference yield:

: 2393-23-9
4-methoxy-benzylamine

: 90521-21-4
3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: 74 percent / H₂O / 0.25 h / Ambient temperature

2: H₂ / Raney Ni / ethanol / 5 h / 25 °C / 2280 Torr

3: 65 percent / 2 M aq. HCl, NaNO₂

4: 42 percent / ethyl acetate / 48 h / Ambient temperature

With hydrogenchloride; hydrogen; sodium nitrite; nickel; In ethanol; water; ethyl acetate;
DOI:10.1021/jm00385a018

Reference yield:

: 90521-87-2
5-Nitro-1H-imidazole-4-sulfonic acid 4-methoxy-benzylamide

: 90521-21-4
3-(2-chloroethyl)-8-imidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / Raney Ni / ethanol / 5 h / 25 °C / 2280 Torr

2: 65 percent / 2 M aq. HCl, NaNO₂

3: 42 percent / ethyl acetate / 48 h / Ambient temperature

With hydrogenchloride; hydrogen; sodium nitrite; nickel; In ethanol; ethyl acetate;
DOI:10.1021/jm00385a018