(R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate

Base Information

• Chemical Name: (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate
• CAS No.: 1313412-63-3
• Molecular Formula: C₂₂H₃₁N₅O₃
• Molecular Weight: 413.52
• Mol file: 1313412-63-3.mol

Synonyms:(R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate

Chemical Property of (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate

There total 7 articles about (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate 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: 63.0%

4-(benzyloxymethyl)-6-chloropyrimidin-2-amine (1313412-62-2) + tert-butyl [(3R)-pyrrolidin-3-yl]methylcarbamate (392338-15-7) → (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate (1313412-63-3)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In ethanol; Reflux;

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate (1313412-63-3)

Guidance literature:

Multi-step reaction with 4 steps

1.1: sodium hydride / diethyl ether; mineral oil / 1 h / 20 °C

1.2: 20 °C

2.1: sodium methylate / ethanol / Reflux

3.1: trichlorophosphate / 1,4-dioxane / 70 °C

3.2: pH 7

4.1: N-ethyl-N,N-diisopropylamine / ethanol / Reflux

With sodium methylate; sodium hydride; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In 1,4-dioxane; diethyl ether; ethanol; mineral oil;

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → (R)tert-butyl 1-(2-amino-6-(benzyloxymethyl)pyrimidin-4-yl)pyrroIidin-3yl(methyl)carbamate (1313412-63-3)

Guidance literature:

Multi-step reaction with 3 steps

1: dichloromethane / 18 h / 0 - 20 °C

2: ammonium formate / water; methanol / 5 h / Reflux

3: N-ethyl-N,N-diisopropylamine / ethanol / Reflux

With ammonium formate; N-ethyl-N,N-diisopropylamine; In methanol; ethanol; dichloromethane; water;

upstream raw materials:

benzyl alcohol

di-tert-butyl dicarbonate

(1-benzyl-(3R)-pyrrolidin-3-yl)methylcarbamic acid tert-butyl ester

4-(benzyloxymethyl)-6-chloropyrimidin-2-amine