ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate

Base Information

• Chemical Name: ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate
• CAS No.: 878005-34-6
• Molecular Formula: C₁₇H₁₈N₄O₃S
• Molecular Weight: 358.421
• Mol file: 878005-34-6.mol

Synonyms:ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate

Chemical Property of ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate

There total 2 articles about ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]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:

2-amino-6-ethyl-3,7-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidine (878005-33-5) + diethyl 4,4'-dithiobis (20057-83-4) → ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate (878005-34-6)

Guidance literature:

diethyl 4,4'-dithiobis; With sodium tetrahydroborate; In ethanol; for 0.5h;

2-amino-6-ethyl-3,7-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidine; With iodine; In ethanol; water; at 100 ℃; for 4h;

DOI:10.1021/jm058276a

Reference yield:

4,4'-Dithiobisbenzoic acid (1155-51-7) → ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate (878005-34-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: NaHCO₃ / N,N-dimethyl-acetamide / 120 h / 20 °C

2.1: NaBH₄ / ethanol / 0.5 h

2.2: 470 mg / I₂ / ethanol; H₂O / 4 h / 100 °C

With sodium tetrahydroborate; sodium hydrogencarbonate; In ethanol; N,N-dimethyl acetamide;

DOI:10.1021/jm058276a

Reference yield: 75.0%

ethyl 4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)sulfanyl]benzoate (878005-34-6) → 4-(2-amino-6-ethyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-ylsulfanyl)-benzoic acid (878005-35-7)

Guidance literature:

With sodium hydroxide; In ethanol; at 80 ℃; for 16h;

DOI:10.1021/jm058276a

upstream raw materials:

2-amino-6-ethyl-3,7-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidine

diethyl 4,4'-dithiobis

4,4'-Dithiobisbenzoic acid

Downstream raw materials:

4-(2-amino-6-ethyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-ylsulfanyl)-benzoic acid

diethyl N-[4-[(2-amino-6-ethyl-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)thio]benzoyl]-L-glutamate