(6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

Base Information

Chemical Name:(6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine
CAS No.:1228649-72-6
Molecular Formula:C₂₅H₂₅F₃N₆
Molecular Weight:466.509
Hs Code.:

(6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

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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 (6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

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Technology Process of (6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

There total 9 articles about (6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]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: 10.0%

: 916764-85-7
(6aR,9aS)-5,6a,7,8,9,9a-hexahydro-5-methyl-3-phenylamino-2-(4-(trifluoromethyl)benzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(2H)-one

: 1228649-72-6
(6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

Guidance literature:: With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 20 ℃; for 72h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.5b01751

Reference yield:

: C₂₅H₂₅F₃N₆O₂

: 1228649-72-6
(6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / dichloromethane / 0 - 20 °C / Inert atmosphere

2: diisobutylaluminium hydride / tetrahydrofuran; toluene / 72 h / 20 °C / Inert atmosphere

With thionyl chloride; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/acs.jmedchem.5b01751

Reference yield:

: C₂₀H₁₅ClF₃N₅O

: 1228649-72-6
(6aR,9aS)-2,4,5,6a,7,8,9,9a-octahydro-5-methyl-3-phenylamino-2-(4-trifluoromethylbenzyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 110 °C / Inert atmosphere

2: thionyl chloride / dichloromethane / 0 - 20 °C / Inert atmosphere

3: diisobutylaluminium hydride / tetrahydrofuran; toluene / 72 h / 20 °C / Inert atmosphere

With thionyl chloride; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/acs.jmedchem.5b01751