(S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

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Chemical Name:(S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine
CAS No.:271247-49-5
Molecular Formula:C₃₆H₃₃F₃N₆O₂
Molecular Weight:638.692
Hs Code.:

Synonyms:(S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

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Chemical Property of (S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

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Technology Process of (S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

There total 7 articles about (S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine 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: 94.0%

: 2627-86-3
(S)-1-phenyl-ethylamine

: 271247-48-4
3-(2-methylsulfonylpyrimidin-4-yl)-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

: 271247-49-5
(S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

Guidance literature:: at 125 ℃; for 3h;
DOI:10.1016/S0960-894X(01)00834-4

Reference yield:

: 705-29-3
3-Trifluoromethylbenzyl chloride

: 271247-49-5
(S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

Guidance literature:: Multi-step reaction with 6 steps

1.1: Mg; I₂ / diethyl ether / 0.5 h / Heating

1.2: 15 percent / diethyl ether / 4 h / Heating

2.1: NaH / dimethylsulfoxide / 0.25 h / 20 °C

2.2: 21 percent / dimethylsulfoxide / 18 h / 20 °C

3.1: N₂H₄ / ethanol / 5 h / 20 °C

4.1: DDQ / toluene / 0.5 h / 20 °C

5.1: 49 percent / 30 percent H₂O₂; Na₂WO₄*2H₂O / methanol; ethyl acetate / 18 h / Heating

6.1: 94 percent / 3 h / 125 °C

With sodium tungstate; dihydrogen peroxide; iodine; sodium hydride; magnesium; 2,3-dicyano-5,6-dichloro-p-benzoquinone; hydrazine; In methanol; diethyl ether; ethanol; dimethyl sulfoxide; ethyl acetate; toluene;
DOI:10.1016/S0960-894X(01)00834-4

Reference yield:

: 271247-59-7
2-methylsulfanyl-pyrimidine-4-carboxylic acid methoxy-methyl-amide

: 271247-49-5
(S)-3-[2-(α-methylbenzylamino)pyrimidin-4-yl]-4-(3-trifluoromethylphenyl)-6-(N-carbobenzoxypiperidin-4-yl)pyridazine

Guidance literature:: Multi-step reaction with 6 steps

1.1: Mg; I₂ / diethyl ether / 0.5 h / Heating

1.2: 15 percent / diethyl ether / 4 h / Heating

2.1: NaH / dimethylsulfoxide / 0.25 h / 20 °C

2.2: 21 percent / dimethylsulfoxide / 18 h / 20 °C

3.1: N₂H₄ / ethanol / 5 h / 20 °C

4.1: DDQ / toluene / 0.5 h / 20 °C

5.1: 49 percent / 30 percent H₂O₂; Na₂WO₄*2H₂O / methanol; ethyl acetate / 18 h / Heating

6.1: 94 percent / 3 h / 125 °C

With sodium tungstate; dihydrogen peroxide; iodine; sodium hydride; magnesium; 2,3-dicyano-5,6-dichloro-p-benzoquinone; hydrazine; In methanol; diethyl ether; ethanol; dimethyl sulfoxide; ethyl acetate; toluene;
DOI:10.1016/S0960-894X(01)00834-4