7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

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Chemical Name:7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine
CAS No.:1350352-16-7
Molecular Formula:C₂₃H₁₄BrF₄N₅OS
Molecular Weight:564.361
Hs Code.:

Synonyms:7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

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Chemical Property of 7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

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Technology Process of 7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

There total 6 articles about 7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine 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: 35.0%

: 1350351-83-5
7-bromo-6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine

: 1350351-94-8
methanesulfonic acid [5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-yl]methanyl ester

: 1350352-16-7
7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

Guidance literature:: In N,N-dimethyl-formamide; at 65 - 85 ℃; for 18h;

Reference yield:

: 1350351-92-6
2-(4-methoxy-2-trifluoromethylphenyl)-5-triisopropylsilanyloxymethyl-[1,3,4]thiadiazole

: 1350352-16-7
7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C

2: pyridine / dichloromethane / 1 h / 20 °C

3: N,N-dimethyl-formamide / 18 h / 65 - 85 °C

With pyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 3438-61-7
5-amino-4-methylpyrimidine

: 1350352-16-7
7-bromo-6-(2-fluorophenyl)-3-[5-(4-methoxy-2-trifluoromethylphenyl)-[1,3,4]thiadiazol-2-ylmethyl]-3H-pyrrolo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran / 3.67 h / -20 - 20 °C

1.2: 1.5 h / -40 - 20 °C

2.1: N-Bromosuccinimide / acetone / 2 h / 20 °C

3.1: N,N-dimethyl-formamide / 18 h / 65 - 85 °C

With N-Bromosuccinimide; n-butyllithium; In tetrahydrofuran; N,N-dimethyl-formamide; acetone;