9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

Base Information

Chemical Name:9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride
CAS No.:75065-17-7
Molecular Formula:C₁₇H₁₅N₂O*Cl
Molecular Weight:298.772
Hs Code.:

Synonyms:9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

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Chemical Property of 9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

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Technology Process of 9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

There total 3 articles about 9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride 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: 96.2%

: 75065-09-7
2-(γ-chloropropyl)-1-phenyl-4(1H)-quinazolinone

: 75065-17-7
9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

Guidance literature:: In chloroform; for 52h; Ambient temperature;
DOI:10.1248/cpb.28.702

Reference yield: 88.0%

: 66491-82-5
2-cyclopropyl-1-phenyl-4(1H)-quinazolinone

: 75065-17-7
9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

Guidance literature:: With hydrogenchloride; In dichloromethane; for 50h; Heating;
DOI:10.1248/cpb.28.702

Reference yield:

: 1211-19-4
2-phenylaminobenzamide

: 75065-17-7
9-Oxo-4-phenyl-2,3,4,9-tetrahydro-1H-pyrrolo[2,1-b]quinazolin-10-ylium; chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / CHCl₃ / 28 h / Ambient temperature

2: 88 percent / HCl / CH₂Cl₂ / 50 h / Heating

With hydrogenchloride; In dichloromethane; chloroform;
DOI:10.1248/cpb.28.702