4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

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Chemical Name:4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide
CAS No.:1269667-16-4
Molecular Formula:C₁₇H₁₇F₂N₅O₃S₂
Molecular Weight:441.482
Hs Code.:

Synonyms:4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

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Chemical Property of 4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

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Technology Process of 4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

There total 4 articles about 4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide 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: 30.0%

: 1269667-81-3
N-(2,6-difluoro-3-(N-(4-methoxybenzyl)propylsulfonylamido)phenyl)-4-(2,4-dimethoxybenzylamino)-5-methylthieno[3,4-d]pyrimidine-7-carboxamide

: 1269667-16-4
4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

Guidance literature:: N-(2,6-difluoro-3-(N-(4-methoxybenzyl)propylsulfonylamido)phenyl)-4-(2,4-dimethoxybenzylamino)-5-methylthieno[3,4-d]pyrimidine-7-carboxamide; With trifluoroacetic acid; for 3h; Reflux;

With sodium hydrogencarbonate; In ethyl acetate;

Reference yield:

: 120651-05-0
α-cyano-β-dimethylaminocrotonamide

: 1269667-16-4
4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / ethanol / Reflux

2.1: acetic anhydride / 4 h / 135 °C

3.1: 2,6-dimethylpyridine; trichlorophosphate / acetonitrile / 4 h / 50 °C

3.2: 1.5 h / 20 °C

4.1: water; lithium hydroxide / tetrahydrofuran / 1 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 55 °C

6.1: trifluoroacetic acid / 3 h / Reflux

With 2,6-dimethylpyridine; water; acetic anhydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; trichlorophosphate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1269667-46-0
ethyl 4-(2,4-dimethoxybenzylamino)-5-methylthieno[3,4-d]pyrimidine-7-carboxylate

: 1269667-16-4
4-amino-5-methylthieno[3,4-d]pyrimidine-7-carboxylic acid [2,6-difluoro-3-(propane-1-sulfonylamino)phenyl]amide

Guidance literature:: Multi-step reaction with 3 steps

1: water; lithium hydroxide / tetrahydrofuran / 1 h / 20 °C

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 55 °C

3: trifluoroacetic acid / 3 h / Reflux

With water; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide;