2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

Base Information

Chemical Name:2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one
CAS No.:197895-97-9
Molecular Formula:C₁₈H₁₇ClN₂OS
Molecular Weight:344.865
Hs Code.:

Synonyms:2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

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Chemical Property of 2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

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Technology Process of 2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

There total 6 articles about 2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-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: 79.0%

: 197895-95-7
2-(2-Chloro-acetylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid m-tolylamide

: 197895-97-9
2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; 1.) 4 h; 2.) reflux, 4 h;

Reference yield:

: 54153-19-4
2-cyano-N-m-tolylacetamide

: 197895-97-9
2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium acetate, glacial acetic acid / benzene / 10 h / Heating

2: sulphur, diethylamine / ethanol / 1 h / 45 - 50 °C

3: 96 percent / acetic acid / 5 h / Heating

4: 79 percent / 1.) HCl gas / dioxane / 1.) 4 h; 2.) reflux, 4 h

With ammonium acetate; hydrogenchloride; sulfur; acetic acid; diethylamine; In 1,4-dioxane; ethanol; acetic acid; benzene;

Reference yield:

: 89733-15-3
α-(N-m-tolylcarboxamide)-α-cyclohexylidene acetonitrile

: 197895-97-9
2-Chloromethyl-3-m-tolyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: sulphur, diethylamine / ethanol / 1 h / 45 - 50 °C

2: 96 percent / acetic acid / 5 h / Heating

3: 79 percent / 1.) HCl gas / dioxane / 1.) 4 h; 2.) reflux, 4 h

With hydrogenchloride; sulfur; diethylamine; In 1,4-dioxane; ethanol; acetic acid;