N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

Base Information

Chemical Name:N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide
CAS No.:1456890-20-2
Molecular Formula:C₁₅H₁₁N₃O₃S
Molecular Weight:313.337
Hs Code.:

Synonyms:N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

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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 N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

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Technology Process of N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

There total 7 articles about N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide 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: 91.0%

: 1456890-19-9
C₁₇H₁₅N₃O₄S

: 1456890-20-2
N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 0 - 20 ℃; for 1h; Inert atmosphere;
DOI:10.1021/jm400718n

Reference yield:

: 844502-63-2
3-ethyl 4-methyl 2-aminothiophene-3,4-dicarboxylate

: 1456890-20-2
N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 70 h / Inert atmosphere; Reflux

2: triethylamine / ethanol / 12 h / Inert atmosphere; Reflux

3: hydrogenchloride / 1,4-dioxane / 1 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; triethylamine; In 1,4-dioxane; ethanol;
DOI:10.1021/jm400718n

Reference yield:

: 66739-89-7
4-(1,3-dioxolan-2-yl)benzonitrile

: 1456890-20-2
N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 - 20 °C / Inert atmosphere

2: triethylamine / ethanol / 12 h / Inert atmosphere; Reflux

3: hydrogenchloride / 1,4-dioxane / 1 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1021/jm400718n