2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Base Information

Chemical Name:2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine
CAS No.:1362709-98-5
Molecular Formula:C₁₈H₁₆FN₅OS
Molecular Weight:369.422
Hs Code.:

Synonyms:2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Suppliers and Price of 2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

There total 6 articles about 2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine 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: 3.0%

: 75-09-2
dichloromethane

: 1362709-72-5
(4-fluorophenyl)(4-(5-methyl-1H-pyrazol-3-ylamino)thieno[3,2-d]pyrimidin-2-yl)methanol

: 1362709-98-5
2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: With phosphorus tribromide; In 1,2-dichloro-ethane; at 60 ℃; for 1h;

Reference yield:

: 319442-18-7
ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate

: 1362709-98-5
2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 8 h / -40 - 40 °C

2: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 70 °C

3: sodium tetrahydroborate / tetrahydrofuran; methanol / 2 h

4: phosphorus tribromide / 1,2-dichloro-ethane / 1 h / 60 °C

With sodium tetrahydroborate; phosphorus tribromide; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 22288-78-4
Methyl 3-aminothiophene-2-carboxylate

: 1362709-98-5
2-((4-fluorophenyl)(methoxy)methyl)-N-(5-methyl-1H-pyrazol-3-yl)thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride / water; acetic acid / 3 h / 70 °C

2: trichlorophosphate / 105 °C

3: tetrahydrofuran / 8 h / -40 - 40 °C

4: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 70 °C

5: sodium tetrahydroborate / tetrahydrofuran; methanol / 2 h

6: phosphorus tribromide / 1,2-dichloro-ethane / 1 h / 60 °C

With hydrogenchloride; sodium tetrahydroborate; phosphorus tribromide; N-ethyl-N,N-diisopropylamine; potassium iodide; trichlorophosphate; In tetrahydrofuran; methanol; water; acetic acid; 1,2-dichloro-ethane; N,N-dimethyl-formamide;