2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

Base Information

Chemical Name:2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol
CAS No.:1161076-34-1
Molecular Formula:C₁₉H₂₁FN₆O
Molecular Weight:368.414
Hs Code.:

Synonyms:2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

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Chemical Property of 2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

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Technology Process of 2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

There total 5 articles about 2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol 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:

: 1161076-94-3
phenylmethyl 2-(4-fluorophenyl)-5,6-dihydro-3-[2-[(2-hydroxy-1-methylethyl)amino]-4-pyrimidinyl]pyrazolo[1,5-b]pyridazine-7(4H)-carboxylate

: 1161076-34-1
2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; for 2h; under 750.075 Torr; Inert atmosphere;

Reference yield:

: 474511-91-6
4-[(4-fluorophenyl)ethynyl]-2-(methylthio)pyrimidine

: 1161076-34-1
2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

Guidance literature:: Multi-step reaction with 4 steps

1: 1,3,5-trimethyl-benzene / 18 h / 165 °C

2: 1,3,5-trimethyl-benzene / 4 h / 140 °C

3: chloroform / 1 h / 120 °C / Sealed tube; Microwave irradiation

4: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C / 750.08 Torr / Inert atmosphere

With hydrogen; palladium 10% on activated carbon; In methanol; chloroform; 1,3,5-trimethyl-benzene;

Reference yield:

: 766-98-3
1-ethynyl-4-fluorobenzene

: 1161076-34-1
2-[[4-[2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-b]pyridazin-3-yl]-2-pyrimidinyl]amino]-1-propanol

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / 18 h / 20 °C / Inert atmosphere

2: 1,3,5-trimethyl-benzene / 18 h / 165 °C

3: 1,3,5-trimethyl-benzene / 4 h / 140 °C

4: chloroform / 1 h / 120 °C / Sealed tube; Microwave irradiation

5: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C / 750.08 Torr / Inert atmosphere

With hydrogen; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium 10% on activated carbon; In methanol; chloroform; 1,3,5-trimethyl-benzene;