di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

Base Information

Chemical Name:di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate
CAS No.:289677-49-2
Molecular Formula:C₃₀H₄₁N₇O₆
Molecular Weight:595.699
Hs Code.:

Synonyms:di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

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Chemical Property of di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

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Technology Process of di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

There total 6 articles about di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]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: 61.0%

: 32677-01-3
L-glutamic acid di-tert-butyl ester hydrochloride

: 289677-48-1
4-{4-[2-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-yl)-ethyl]-imidazol-1-ylmethyl}-benzoic acid

: 289677-49-2
di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

Guidance literature:: With sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 25 ℃; for 12h;
DOI:10.1016/S0968-0896(00)00051-1

Reference yield:

: 2417-72-3
Methyl 4-(bromomethyl)benzoate

: 289677-49-2
di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

Guidance literature:: Multi-step reaction with 5 steps

1: 44 percent / K₂CO₃ / dimethylformamide / 3 h / 100 °C

2: 56 percent / K₂CO₃ / dimethylformamide / 3 h / 70 °C

3: 62 percent / NaOEt / 3 h / 25 °C

4: 81 percent / LiOH; H₂O / methanol / 5 h / 60 °C

5: 61 percent / NaHCO₃; EDCI / dimethylformamide / 12 h / 25 °C

With lithium hydroxide; water; sodium ethanolate; sodium hydrogencarbonate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; N,N-dimethyl-formamide; 1: Alkylation / 2: Alkylation / 3: cyclocondensation; transesterification / 4: Hydrolysis / 5: Acylation;
DOI:10.1016/S0968-0896(00)00051-1

Reference yield:

: 13518-55-3
4-(2-chloroethyl)-1H-imidazole

: 289677-49-2
di-tert-butyl N-{4-[[4-[(2,4-diamino-6(1H)-pyrimidinon-5-yl)ethyl]-1H-imidazol-1-yl]methyl]benzoyl}-L-glutamate

Guidance literature:: Multi-step reaction with 5 steps

1: 44 percent / K₂CO₃ / dimethylformamide / 3 h / 100 °C

2: 56 percent / K₂CO₃ / dimethylformamide / 3 h / 70 °C

3: 62 percent / NaOEt / 3 h / 25 °C

4: 81 percent / LiOH; H₂O / methanol / 5 h / 60 °C

5: 61 percent / NaHCO₃; EDCI / dimethylformamide / 12 h / 25 °C

With lithium hydroxide; water; sodium ethanolate; sodium hydrogencarbonate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; N,N-dimethyl-formamide; 1: Alkylation / 2: Alkylation / 3: cyclocondensation; transesterification / 4: Hydrolysis / 5: Acylation;
DOI:10.1016/S0968-0896(00)00051-1