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2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic acid

Base Information Edit
  • Chemical Name:2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic acid
  • CAS No.:1303968-87-7
  • Molecular Formula:C27H20N4O5S
  • Molecular Weight:512.546
  • Hs Code.:
  • Mol file:1303968-87-7.mol
2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic acid

Synonyms:2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic acid

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Chemical Property of 2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic acid Edit
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Technology Process of 2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic acid

There total 7 articles about 2-phenyl-3-(4'-[N-(4''-aminophenyl)carbamoyl]-phenyl)-quinazoline-4(3H)-one-6-sulphonic 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:
Guidance literature:
2-phenyl-4-oxo-3,1-benzoxazine-6-sulphonic acid; 4,4'-diaminobenzanilide; With pyridine; for 6h; Reflux;
With hydrogenchloride; In water; at 20 ℃;
DOI:10.2298/JSC090225021P
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrogenchloride; iron / water / 2 h / 95 - 98 °C
2.1: pyridine / 6 h / Reflux
2.2: 20 °C
With pyridine; hydrogenchloride; iron; In water;
DOI:10.2298/JSC090225021P
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / chlorobenzene / 4.5 h / 90 - 95 °C
2.1: hydrogenchloride; iron / water / 2 h / 95 - 98 °C
3.1: pyridine / 6 h / Reflux
3.2: 20 °C
With pyridine; hydrogenchloride; iron; triethylamine; In water; chlorobenzene;
DOI:10.2298/JSC090225021P
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