1H-Imidazole-1-carboxylic acid, 4-[[1,4-dihydro-1-[2-[[1-(methoxycarbonyl)cyclohexyl]amino]-2-oxoethyl]- 2,4-dioxo-3(2H)-quinazolinyl]methyl]-, 1,1-dimethylethyl ester

Base Information

Chemical Name:1H-Imidazole-1-carboxylic acid, 4-[[1,4-dihydro-1-[2-[[1-(methoxycarbonyl)cyclohexyl]amino]-2-oxoethyl]- 2,4-dioxo-3(2H)-quinazolinyl]methyl]-, 1,1-dimethylethyl ester
CAS No.:847665-26-3
Molecular Formula:C27H33N5O7
Molecular Weight:539.588
Hs Code.:

1H-Imidazole-1-carboxylic acid,
4-[[1,4-dihydro-1-[2-[[1-(methoxycarbonyl)cyclohexyl]amino]-2-oxoethyl]-
2,4-dioxo-3(2H)-quinazolinyl]methyl]-, 1,1-dimethylethyl ester

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Chemical Property of 1H-Imidazole-1-carboxylic acid, 4-[[1,4-dihydro-1-[2-[[1-(methoxycarbonyl)cyclohexyl]amino]-2-oxoethyl]- 2,4-dioxo-3(2H)-quinazolinyl]methyl]-, 1,1-dimethylethyl ester

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Technology Process of 1H-Imidazole-1-carboxylic acid, 4-[[1,4-dihydro-1-[2-[[1-(methoxycarbonyl)cyclohexyl]amino]-2-oxoethyl]- 2,4-dioxo-3(2H)-quinazolinyl]methyl]-, 1,1-dimethylethyl ester

There total 7 articles about 1H-Imidazole-1-carboxylic acid, 4-[[1,4-dihydro-1-[2-[[1-(methoxycarbonyl)cyclohexyl]amino]-2-oxoethyl]- 2,4-dioxo-3(2H)-quinazolinyl]methyl]-, 1,1-dimethylethyl ester 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: 100.0%

: 847665-21-8
4-(1-carboxymethyl-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-ylmethyl)imidazole-1-carboxylic acid tert-butyl ester

: 4507-57-7
methyl 1-aminocyclohexanecarboxylate

: 847665-26-3
4-{1-[(1-(methoxycarbonyl)cyclohexylcarbamoyl)methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-ylmethyl}-imidazole-1-carboxylic acid tert-butyl ester

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.bmc.2004.10.053

Reference yield:

: 500782-71-8
4-(chloromethyl)imidazole-1-carboxylic acid tert-butyl ester

: 847665-26-3
4-{1-[(1-(methoxycarbonyl)cyclohexylcarbamoyl)methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-ylmethyl}-imidazole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / potassium carbonate / acetone / 60 °C

2: 91 percent / hydrogen / Pd/C / methanol; CH₂Cl₂ / 2.5 h

3: 100 percent / 1-hydroxybenzotriazole; Et₃N; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / dimethylformamide / 20 °C

With hydrogen; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmc.2004.10.053

Reference yield:

: 847665-19-4
(2,4-dioxo-3,4-dihydro-2H-quinazolin-1-yl)acetic acid benzyl ester

: 847665-26-3
4-{1-[(1-(methoxycarbonyl)cyclohexylcarbamoyl)methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-ylmethyl}-imidazole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / potassium carbonate / acetone / 60 °C

2: 91 percent / hydrogen / Pd/C / methanol; CH₂Cl₂ / 2.5 h

3: 100 percent / 1-hydroxybenzotriazole; Et₃N; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / dimethylformamide / 20 °C

With hydrogen; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmc.2004.10.053