diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

Base Information

Chemical Name:diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate
CAS No.:1404216-23-4
Molecular Formula:C₂₂H₃₁N₄O₅P
Molecular Weight:462.486
Hs Code.:

Synonyms:diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

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Chemical Property of diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

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Technology Process of diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

There total 5 articles about diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate 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:

: 1166948-81-7
4-benzyloxy-5H-pyrrolo[3,2-d]pyrimidine-7-carbaldehyde

: 1404216-22-3
diethyl [2-(aminomethyl)-3-hydroxypropyl]phosphonate

: 1404216-23-4
diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

Guidance literature:: 4-benzyloxy-5H-pyrrolo[3,2-d]pyrimidine-7-carbaldehyde; diethyl [2-(aminomethyl)-3-hydroxypropyl]phosphonate; In ethanol; at 70 ℃; for 0.166667h;

With 2-picoline borane complex; In ethanol; at 70 ℃; for 2h;

Reference yield:

: 1404216-20-1
C₁₆H₂₇O₇PS

: 1404216-23-4
diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium azide / N,N-dimethyl-formamide / 7 h / 80 °C

2.1: hydrogen / 20% palladium hydroxide-activated charcoal / methanol / 18 h / 760.05 Torr

3.1: ethanol / 0.17 h / 70 °C

3.2: 2 h / 70 °C

With sodium azide; hydrogen; 20% palladium hydroxide-activated charcoal; In methanol; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1404216-18-7
diethyl {2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]propyl}phosphonate

: 1404216-23-4
diethyl {2-[({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yl]methyl}amino)methyl]-3-hydroxypropyl}phosphonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / water; methanol / 1 h / 20 °C

2.1: triethylamine / dichloromethane / 1 h / 0 - 20 °C

3.1: sodium azide / N,N-dimethyl-formamide / 7 h / 80 °C

4.1: hydrogen / 20% palladium hydroxide-activated charcoal / methanol / 18 h / 760.05 Torr

5.1: ethanol / 0.17 h / 70 °C

5.2: 2 h / 70 °C

With hydrogenchloride; sodium azide; hydrogen; triethylamine; 20% palladium hydroxide-activated charcoal; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;