ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

Base Information

Chemical Name:ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate
CAS No.:165900-67-4
Molecular Formula:C₂₂H₂₈N₆O₅
Molecular Weight:456.502
Hs Code.:

ethyl 4-<N-<2-(2,4-diamino-6-oxo-6,7-dihydro-5H-pyrrolo<2,3-d>pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

Synonyms:ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

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Chemical Property of ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

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Technology Process of ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

There total 1 articles about ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate 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: 85.0%

: 50-01-1
guanidine hydrochloride

: 109-77-3
malononitrile

: 165900-67-4
ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

Guidance literature:: With sodium ethanolate; In tetrahydrofuran; ethanol; for 3h; Heating;
DOI:10.1248/cpb.43.256

Reference yield: 86.0%

: 165900-67-4
ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

: 165900-68-5
ethyl 4-pyrimidin-5-yl)ethyl>amino>benzoate

Guidance literature:: With trifluoroacetic acid; for 1h;
DOI:10.1248/cpb.43.256

Reference yield:

: 165900-67-4
ethyl 4-pyrimidin-5-yl)ethyl>-N-(tert-butoxycarbonyl)amino>benzoate

: 133719-61-6
ethyl 4-pyrimidin-5-yl)ethyl>amino>benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / TFA / 1 h

2: 24 percent / BH₃*THF / tetrahydrofuran / 6 h / 0 °C

With borane-THF; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1248/cpb.43.256