4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

Base Information

Chemical Name:4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid
CAS No.:289677-32-3
Molecular Formula:C₁₆H₁₆N₆O₃
Molecular Weight:340.341
Hs Code.:

Synonyms:4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

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Chemical Property of 4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

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Technology Process of 4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

There total 5 articles about 4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid 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: 84.0%

: 289677-31-2
4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid ethyl ester

: 289677-32-3
4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

Guidance literature:: With lithium hydroxide; water; In methanol; at 60 ℃; for 5h;
DOI:10.1016/S0968-0896(00)00051-1

Reference yield:

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

: 289677-32-3
4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 49 percent / K₂CO₃ / dimethylformamide / 3 h / 100 °C

2: 89 percent / thionyl chloride / CH₂Cl₂ / 3 h / 40 °C

3: 76 percent / K₂CO₃ / dimethylformamide / 3 h / 70 °C

4: 62 percent / NaOEt / 3 h / 25 °C

5: 84 percent / LiOH; H₂O / methanol / 5 h / 60 °C

With lithium hydroxide; thionyl chloride; water; sodium ethanolate; potassium carbonate; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: Alkylation / 2: Chlorination / 3: Alkylation / 4: cyclocondensation; transesterification / 5: Hydrolysis;
DOI:10.1016/S0968-0896(00)00051-1

Reference yield:

: 289677-29-8
methyl 4-[(4-chloromethyl-1H-imidazol-1-yl)methyl]benzoate

: 289677-32-3
4-[4-(2,4-diamino-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-imidazol-1-ylmethyl]-benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / K₂CO₃ / dimethylformamide / 3 h / 70 °C

2: 62 percent / NaOEt / 3 h / 25 °C

3: 84 percent / LiOH; H₂O / methanol / 5 h / 60 °C

With lithium hydroxide; water; sodium ethanolate; potassium carbonate; In methanol; N,N-dimethyl-formamide; 1: Alkylation / 2: cyclocondensation; transesterification / 3: Hydrolysis;
DOI:10.1016/S0968-0896(00)00051-1