diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

Base Information

Chemical Name:diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate
CAS No.:149765-22-0
Molecular Formula:C₂₉H₃₇N₅O₆
Molecular Weight:551.643
Hs Code.:

Synonyms:diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

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Chemical Property of diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

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Technology Process of diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

There total 6 articles about diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate 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: 59.0%

: 149765-17-3
diethyl N-<2-pivaloylamino-4-chloro<(pyrrolo<2,3-d>pyrimidin-5-yl)ethynyl>benzoyl>-L-glutamate

: 149765-22-0
diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

Guidance literature:: With ammonium hydroxide; hydrogen; palladium on activated charcoal; In ethanol; dichloromethane; for 20h; under 2585.7 Torr;
DOI:10.3987/COM-92-S(T)65

Reference yield:

: 3282-30-2
pivaloyl chloride

: 149765-22-0
diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / pyridine / 0.5 h / Ambient temperature

2: 83 percent / N-iodosuccinimide / tetrahydrofuran / 1 h / Ambient temperature

3: 58 percent / copper(I) iodide, tetrakis(triphenylphosphine)palladium⁽⁰⁾, triethylamine / dimethylformamide / 4 h / Ambient temperature

4: 59 percent / H₂, NH₄OH / 10percent Pd/C / ethanol; CH₂Cl₂ / 20 h / 2585.7 Torr

With pyridine; ammonium hydroxide; N-iodo-succinimide; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.3987/COM-92-S(T)65

Reference yield:

: 84955-31-7
4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine

: 149765-22-0
diethyl N-<2-pivaloylamino<(pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>benzoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / pyridine / 0.5 h / Ambient temperature

2: 83 percent / N-iodosuccinimide / tetrahydrofuran / 1 h / Ambient temperature

3: 58 percent / copper(I) iodide, tetrakis(triphenylphosphine)palladium⁽⁰⁾, triethylamine / dimethylformamide / 4 h / Ambient temperature

4: 59 percent / H₂, NH₄OH / 10percent Pd/C / ethanol; CH₂Cl₂ / 20 h / 2585.7 Torr

With pyridine; ammonium hydroxide; N-iodo-succinimide; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.3987/COM-92-S(T)65