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4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-carboxamide

Base Information Edit
  • Chemical Name:4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-carboxamide
  • CAS No.:1379545-91-1
  • Molecular Formula:C20H20FN5O
  • Molecular Weight:365.41
  • Hs Code.:
  • Mol file:1379545-91-1.mol
4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-carboxamide

Synonyms:4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-carboxamide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-carboxamide Edit
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Technology Process of 4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-carboxamide

There total 8 articles about 4-[(S)-2-azetidin-1-yl-1-(3-fluorophenyl)-ethylamino]-quinazoline-8-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:
Guidance literature:
Multi-step reaction with 5 steps
1.1: 4 h / 140 °C
2.1: ammonium hydroxide; ammonium acetate / 2 h / 80 °C
2.2: 72 h / 80 °C / pressure bottle
3.1: sulfuric acid / Inert atmosphere; Reflux
4.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride / acetonitrile / 90 °C
5.1: N-ethyl-N,N-diisopropylamine; sodium sulfate / acetonitrile / 0.17 h
5.2: 45 - 60 °C
5.3: 18 h / 60 °C / pressure vessel
With ammonium hydroxide; sulfuric acid; ammonium acetate; N-benzyl-N,N,N-triethylammonium chloride; sodium sulfate; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In acetonitrile;
Guidance literature:
C11H15FN2*2ClH; With sodium sulfate; N-ethyl-N,N-diisopropylamine; In acetonitrile; for 0.166667h;
4-chloro-quinazoline-8-carboxylic acid methyl ester; In acetonitrile; at 45 - 60 ℃;
With ammonia; In methanol; at 60 ℃; for 18h; pressure vessel;
Guidance literature:
Multi-step reaction with 4 steps
1.1: thionyl chloride; pyridine / acetonitrile / -40 - 20 °C
1.2: 18 h / 20 °C
2.1: acetonitrile / 20 °C
3.1: hydrogenchloride / diethyl ether; methanol / 3 h / 20 °C
4.1: N-ethyl-N,N-diisopropylamine; sodium sulfate / acetonitrile / 0.17 h
4.2: 45 - 60 °C
4.3: 18 h / 60 °C / pressure vessel
With pyridine; hydrogenchloride; thionyl chloride; sodium sulfate; N-ethyl-N,N-diisopropylamine; In methanol; diethyl ether; acetonitrile;
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