(R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Base Information

Chemical Name:(R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
CAS No.:1589536-76-4
Molecular Formula:C₁₇H₂₀N₆O₂
Molecular Weight:340.385
Hs Code.:

Synonyms:(R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

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Chemical Property of (R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

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Technology Process of (R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

There total 4 articles about (R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea 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:

: 1185190-81-1
4,6-dichloro-2-methyl-3-cyanopyridine

: 1589536-76-4
(R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 16 h / 75 °C / Sealed tube

2: silver(I) tetrafluoroborate / 17 h / 50 °C

3: C₅₁H₄₂ClNOP₂Pd; triethylsilane / tetrahydrofuran / 17 h / 50 °C / Sealed tube; Inert atmosphere

4: hydrazine hydrate / ethanol / 18 h / 100 °C / Sealed tube

With triethylsilane; N-Bromosuccinimide; hydrazine hydrate; 2,2'-azobis(isobutyronitrile); silver(I) tetrafluoroborate; C₅₁H₄₂ClNOP₂Pd; In tetrahydrofuran; tetrachloromethane; ethanol;

Reference yield:

: 64169-92-2
4-hydroxy-2-methyl-6-oxo-1,6-dihydropyridine-3-carbonitrile

: 1589536-76-4
(R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate / N,N-dimethyl-formamide / 17 h / 90 °C

2: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 16 h / 75 °C / Sealed tube

3: silver(I) tetrafluoroborate / 17 h / 50 °C

4: C₅₁H₄₂ClNOP₂Pd; triethylsilane / tetrahydrofuran / 17 h / 50 °C / Sealed tube; Inert atmosphere

5: hydrazine hydrate / ethanol / 18 h / 100 °C / Sealed tube

With triethylsilane; N-Bromosuccinimide; hydrazine hydrate; 2,2'-azobis(isobutyronitrile); silver(I) tetrafluoroborate; C₅₁H₄₂ClNOP₂Pd; trichlorophosphate; In tetrahydrofuran; tetrachloromethane; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1589541-05-8
4,6-dichloro-2-(methoxymethyl)nicotinonitrile

: 1589536-76-4
(R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: C₅₁H₄₂ClNOP₂Pd; triethylsilane / tetrahydrofuran / 17 h / 50 °C / Sealed tube; Inert atmosphere

2: hydrazine hydrate / ethanol / 18 h / 100 °C / Sealed tube

With triethylsilane; hydrazine hydrate; C₅₁H₄₂ClNOP₂Pd; In tetrahydrofuran; ethanol;