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(S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride

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  • Chemical Name:(S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride
  • CAS No.:1359669-09-2
  • Molecular Formula:C26H31N7O2*ClH
  • Molecular Weight:510.039
  • Hs Code.:
  • Mol file:1359669-09-2.mol
(S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride

Synonyms:(S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride

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Chemical Property of (S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride Edit
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Technology Process of (S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride

There total 6 articles about (S)-2-phenyl-5,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid {2-[(2-cyanopyrrolidin-1-yl)-2-oxoethylamino]-2-methylpropyl}amide hydrochloride 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:
(S)-1-(2-((1-amino-2-methylpropan-2-yl)amino)acetyl)pyrrolidine-2-carbonitrile; C19H15N5O3; With triethylamine; In tetrahydrofuran; at 20 ℃; Cooling with ice;
With hydrogenchloride; In 1,4-dioxane; water; at 10 ℃; for 0.166667h;
DOI:10.1016/j.bmc.2011.09.043
Guidance literature:
Multi-step reaction with 2 steps
1.1: tetrahydrofuran / 4 h / 20 °C
2.1: triethylamine / tetrahydrofuran / 20 °C / Cooling with ice
2.2: 0.17 h / 10 °C
With triethylamine; In tetrahydrofuran;
DOI:10.1016/j.bmc.2011.09.043
Guidance literature:
Multi-step reaction with 3 steps
1.1: acetic acid / 3 h / 120 °C
1.2: 1 h / 70 °C
1.3: 20 °C
2.1: tetrahydrofuran / 4 h / 20 °C
3.1: triethylamine / tetrahydrofuran / 20 °C / Cooling with ice
3.2: 0.17 h / 10 °C
With acetic acid; triethylamine; In tetrahydrofuran;
DOI:10.1016/j.bmc.2011.09.043
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