N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

Base Information

Chemical Name:N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide
CAS No.:1310489-86-1
Molecular Formula:C₂₅H₂₄ClN₃O
Molecular Weight:417.938
Hs Code.:

Synonyms:N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

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Chemical Property of N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

Chemical Property:

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Technology Process of N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

There total 6 articles about N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide 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:

: C₃₈H₃₇ClN₃O₂P

: 1310489-86-1
N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

Guidance literature:: In toluene; for 4h; Reflux;
DOI:10.1016/j.tet.2011.03.056

Reference yield:

: 1310489-53-2
N-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide

: 1310489-86-1
N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 2 h

2: toluene / 4 h / Reflux

In toluene; 1: Staudinger reaction / 2: Aza-Wittig reaction;
DOI:10.1016/j.tet.2011.03.056

Reference yield:

: 119072-55-8,7188-38-7
tert-butylisonitrile

: 1310489-86-1
N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / 24 h / 20 °C

2: toluene / 2 h

3: toluene / 4 h / Reflux

In methanol; toluene; 1: Ugi condensation / 2: Staudinger reaction / 3: Aza-Wittig reaction;
DOI:10.1016/j.tet.2011.03.056