Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

Base Information

Chemical Name:Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate
CAS No.:1332758-62-9
Molecular Formula:C₁₉H₂₁FN₄O₅S₂
Molecular Weight:468.53
Hs Code.:

Synonyms:Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

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Chemical Property of Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

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Technology Process of Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

There total 5 articles about Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate 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:

: 1332758-56-1
Methyl 4-(2-(1-aminopropan-2-yloxy)-4-fluorophenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate trifluoroacetate

: 124-63-0
methanesulfonyl chloride

: 1332758-62-9
Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

Guidance literature:: With triethylamine; at 20 ℃;

Reference yield:

: 446-36-6
5-fluoro-2-nitrophenol

: 1332758-62-9
Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: triphenylphosphine; di-tert-butyl-diazodicarboxylate / tetrahydrofuran / 2 h / 20 °C / Cooling with ice

2: hydrogen / palladium 10% on activated carbon / methanol / 20 °C / 2585.81 Torr

3: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 72 h / 100 °C

4: dichloromethane / 2 h / 20 °C

5: triethylamine / 20 °C

With di-tert-butyl-diazodicarboxylate; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; 1: Mitsunobu reaction;

Reference yield:

: 1332721-17-1
[2-(5-fluoro-2-nitro-phenoxy)-propyl]-carbamic acid tert-butyl ester

: 1332758-62-9
Methyl 4-(4-fluoro-(2-(1-methylsulfonamido)propan-2-yloxy)phenylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen / palladium 10% on activated carbon / methanol / 20 °C / 2585.81 Torr

2: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 72 h / 100 °C

3: dichloromethane / 2 h / 20 °C

4: triethylamine / 20 °C

With hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In 1,4-dioxane; methanol; dichloromethane;