(R)-N-(4-(methoxymethyl)-6-(3-(1-phenylethyl)ureido)-1H-pyrazolo[4,3-c]pyridin-3-yl)acetamide

Base Information

Chemical Name:(R)-N-(4-(methoxymethyl)-6-(3-(1-phenylethyl)ureido)-1H-pyrazolo[4,3-c]pyridin-3-yl)acetamide
CAS No.:1589536-79-7
Molecular Formula:C₁₉H₂₂N₆O₃
Molecular Weight:382.422
Hs Code.:

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

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

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

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

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

: 75-36-5
acetyl chloride

: 1589536-79-7
(R)-N-(4-(methoxymethyl)-6-(3-(1-phenylethyl)ureido)-1H-pyrazolo[4,3-c]pyridin-3-yl)acetamide

Guidance literature:: (R)-1-(3-amino-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea; acetyl chloride; With pyridine; In tetrahydrofuran; at 20 ℃; for 17h;

With sodium hydroxide; In tetrahydrofuran; at 20 - 50 ℃; for 3h;

Reference yield:

: 1589541-02-5
2-(bromomethyl)-4,6-dichloronicotinonitrile

: 1589536-79-7
(R)-N-(4-(methoxymethyl)-6-(3-(1-phenylethyl)ureido)-1H-pyrazolo[4,3-c]pyridin-3-yl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

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

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

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

4.1: pyridine / tetrahydrofuran / 17 h / 20 °C

4.2: 3 h / 20 - 50 °C

With pyridine; triethylsilane; hydrazine hydrate; silver(I) tetrafluoroborate; C₅₁H₄₂ClNOP₂Pd; In tetrahydrofuran; ethanol;

Reference yield:

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

: 1589536-79-7
(R)-N-(4-(methoxymethyl)-6-(3-(1-phenylethyl)ureido)-1H-pyrazolo[4,3-c]pyridin-3-yl)acetamide

Guidance literature:: Multi-step reaction with 6 steps

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

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

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

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

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

6.1: pyridine / tetrahydrofuran / 17 h / 20 °C

6.2: 3 h / 20 - 50 °C

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