[(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

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Chemical Name:[(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol
CAS No.:1370007-58-1
Molecular Formula:C₃₆H₄₀N₄O₃Si
Molecular Weight:604.824
Hs Code.:

Synonyms:[(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

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Chemical Property of [(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

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Technology Process of [(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

There total 7 articles about [(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol 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: 21.0%

: 1370007-56-9
[(2R,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]-2,5-dihydrofuran-2-yl]methanol

: 1370007-58-1
[(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

Guidance literature:: With hydrogen; Crabtree's catalyst; In dichloromethane; for 42h; Inert atmosphere;

Reference yield:

: 628733-99-3
ethyl 1-amino-1H-pyrrole-2-carboxylate

: 1370007-58-1
[(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

Guidance literature:: Multi-step reaction with 6 steps

1: 1 h / 200 °C / Microwave irradiation

2: N-Bromosuccinimide; trifluoroacetic acid / dichloromethane / 1.25 h / 0 °C

3: trichlorophosphate / 2 h / 110 °C

4: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.5 h / 100 °C / Microwave irradiation

5: N-ethyl-N,N-diisopropylamine / bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 12 h / 60 °C / Inert atmosphere

6: hydrogen / Crabtree's catalyst / dichloromethane / 42 h / Inert atmosphere

With N-Bromosuccinimide; hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; trichlorophosphate; bis(tri-t-butylphosphine)palladium⁽⁰⁾; Crabtree's catalyst; In tetrahydrofuran; 1,4-dioxane; dichloromethane;

Reference yield:

: 1269667-51-7
7-bromo-4-chloropyrrolo[2,1-f][1,2,4]triazine

: 1370007-58-1
[(2R,3S,5R)-3-(tert-butyl(diphenyl)silyl)oxy-5-[4-[[(1S)-indan-1-yl]amino]pyrrolo[2,1-f][1,2,4]triazin-7-yl]tetrahydrofuran-2-yl]methanol

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.5 h / 100 °C / Microwave irradiation

2: N-ethyl-N,N-diisopropylamine / bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 12 h / 60 °C / Inert atmosphere

3: hydrogen / Crabtree's catalyst / dichloromethane / 42 h / Inert atmosphere

With hydrogen; N-ethyl-N,N-diisopropylamine; bis(tri-t-butylphosphine)palladium⁽⁰⁾; Crabtree's catalyst; In tetrahydrofuran; 1,4-dioxane; dichloromethane;