3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one

Base Information

• Chemical Name: 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one
• CAS No.: 1330780-40-9
• Molecular Formula: C₂₄H₂₇ClN₆O
• Molecular Weight: 450.971

Synonyms:3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one

Chemical Property of 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one

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Technology Process of 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one

There total 3 articles about 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one 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: 89.0%

diisobutylamine (110-96-3) + N-[4-(ethoxycarbonyl)-1-(4'-chloro)phenyl-1,2,3-triazol-5-yl]-N'-phenylcarbodiimide (652986-16-8) → 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one (1330780-40-9)

Guidance literature:

diisobutylamine; N-[4-(ethoxycarbonyl)-1-(4'-chloro)phenyl-1,2,3-triazol-5-yl]-N'-phenylcarbodiimide; In dichloromethane; at 20 ℃;

With alcohol; sodium alkoxide; In dichloromethane; at 20 ℃;

DOI:10.1002/cjoc.201190201

Reference yield:

phenyl isocyanate (103-71-9) → 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one (1330780-40-9)

Guidance literature:

Multi-step reaction with 2 steps

1.1: dichloromethane / 24 h / 20 °C / Inert atmosphere

2.1: dichloromethane / 20 °C

2.2: alcohol; sodium alkoxide / 20 °C

In dichloromethane; 1.1: aza-Wittig reaction;

DOI:10.1002/cjoc.201190201

Reference yield:

1-(p-chlorophenyl)-4-ethoxycarbonyl-5-[(triphenylphosphoranylidene)amino]-1,2,3-triazole (272123-45-2) → 3-(4-chlorophenyl)-5-di(iso-butyl)amino-6-phenyl-3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one (1330780-40-9)

Guidance literature:

Multi-step reaction with 2 steps

1.1: dichloromethane / 24 h / 20 °C / Inert atmosphere

2.1: dichloromethane / 20 °C

2.2: alcohol; sodium alkoxide / 20 °C

In dichloromethane; 1.1: aza-Wittig reaction;

DOI:10.1002/cjoc.201190201

upstream raw materials:

diisobutylamine

N-[4-(ethoxycarbonyl)-1-(4'-chloro)phenyl-1,2,3-triazol-5-yl]-N'-phenylcarbodiimide

phenyl isocyanate

1-(p-chlorophenyl)-4-ethoxycarbonyl-5-[(triphenylphosphoranylidene)amino]-1,2,3-triazole

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