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(R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Base Information
  • Chemical Name:(R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide
  • CAS No.:1364889-60-0
  • Molecular Formula:C18H15F3N6O2
  • Molecular Weight:404.351
  • Hs Code.:
(R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Synonyms:(R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

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Chemical Property of (R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide
Chemical Property:
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Technology Process of (R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

There total 13 articles about (R)-N-carbamoyl-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-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:
With ammonium hydroxide; ammonium chloride; at 20 ℃; for 1h;
Guidance literature:
Multi-step reaction with 8 steps
1.1: triethylamine; methanesulfonyl chloride / dichloromethane / 1 h / -60 °C / Inert atmosphere
2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C
2.2: 20 °C
3.1: trichloroisocyanuric acid / 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / 1.25 h / -10 - 20 °C
4.1: diethylamino-sulfur trifluoride / dichloromethane / 2.5 h / -78 - 20 °C / Plastic bottle
5.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
5.2: 0 °C
6.1: potassium fluoride / dimethyl sulfoxide / 2 h / 85 °C
7.1: 4 h / 85 °C
8.1: ammonium hydroxide; ammonium chloride / 1 h / 20 °C
With potassium fluoride; ammonium hydroxide; diethylamino-sulfur trifluoride; trichloroisocyanuric acid; tetrabutyl ammonium fluoride; ammonium chloride; methanesulfonyl chloride; triethylamine; trifluoroacetic acid; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
Guidance literature:
Multi-step reaction with 6 steps
1.1: trichloroisocyanuric acid / 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / 1.25 h / -10 - 20 °C
2.1: diethylamino-sulfur trifluoride / dichloromethane / 2.5 h / -78 - 20 °C / Plastic bottle
3.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
3.2: 0 °C
4.1: potassium fluoride / dimethyl sulfoxide / 2 h / 85 °C
5.1: 4 h / 85 °C
6.1: ammonium hydroxide; ammonium chloride / 1 h / 20 °C
With potassium fluoride; ammonium hydroxide; diethylamino-sulfur trifluoride; trichloroisocyanuric acid; ammonium chloride; trifluoroacetic acid; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; In dichloromethane; dimethyl sulfoxide;
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