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C58H58ClN8O14P

Base Information
  • Chemical Name:C58H58ClN8O14P
  • CAS No.:83327-02-0
  • Molecular Formula:C58H58ClN8O14P
  • Molecular Weight:1157.57
  • Hs Code.:
C<sub>58</sub>H<sub>58</sub>ClN<sub>8</sub>O<sub>14</sub>P

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Chemical Property of C58H58ClN8O14P
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Technology Process of C58H58ClN8O14P

There total 14 articles about C58H58ClN8O14P 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 2 steps
1: 2.) 2,4,6-triisopropylbenzenesulfonyl chloride / 1.) N-methylimidazole / 2.) pyridine, 30 min
2: hydrazine hydrate / pyridine; acetic acid / 0.75 h
With 2,4,6-triisopropylphenylsulfonyl chloride; hydrazine hydrate; 1-methyl-1H-imidazole; In pyridine; acetic acid;
DOI:10.1016/0040-4020(84)85098-X
Guidance literature:
Multi-step reaction with 10 steps
1: 92 percent / pyridine / 1 h
2: Et3N / 4-dimethylaminopyridine / CH2Cl2 / 2 h / Ambient temperature
3: 1.) Me3N; 2.) NH3 / CH2Cl2 / 1.) 0 deg C; 2.) 5 h, reflux
4: pyridine / 1 h
5: 1.4 g / 1 N NaOH / pyridine; H2O / 0.17 h / 0 °C
6: pyridine / 3 h
7: Et3N, 4-dimethylaminopyridine / diethyl ether; pyridine / Ambient temperature
8: 1.6 g / tetra-n-butylammonium flouride / tetrahydrofuran / 0.5 h
9: 2.) 2,4,6-triisopropylbenzenesulfonyl chloride / 1.) N-methylimidazole / 2.) pyridine, 30 min
10: hydrazine hydrate / pyridine; acetic acid / 0.75 h
With dmap; sodium hydroxide; 2,4,6-triisopropylphenylsulfonyl chloride; tetrabutyl ammonium fluoride; ammonia; hydrazine hydrate; triethylamine; trimethylamine; 1-methyl-1H-imidazole; dmap; In tetrahydrofuran; pyridine; diethyl ether; dichloromethane; water; acetic acid;
DOI:10.1016/0040-4020(84)85098-X
Guidance literature:
Multi-step reaction with 8 steps
1: 1.) Me3N; 2.) NH3 / CH2Cl2 / 1.) 0 deg C; 2.) 5 h, reflux
2: pyridine / 1 h
3: 1.4 g / 1 N NaOH / pyridine; H2O / 0.17 h / 0 °C
4: pyridine / 3 h
5: Et3N, 4-dimethylaminopyridine / diethyl ether; pyridine / Ambient temperature
6: 1.6 g / tetra-n-butylammonium flouride / tetrahydrofuran / 0.5 h
7: 2.) 2,4,6-triisopropylbenzenesulfonyl chloride / 1.) N-methylimidazole / 2.) pyridine, 30 min
8: hydrazine hydrate / pyridine; acetic acid / 0.75 h
With dmap; sodium hydroxide; 2,4,6-triisopropylphenylsulfonyl chloride; tetrabutyl ammonium fluoride; ammonia; hydrazine hydrate; triethylamine; trimethylamine; 1-methyl-1H-imidazole; In tetrahydrofuran; pyridine; diethyl ether; dichloromethane; water; acetic acid;
DOI:10.1016/0040-4020(84)85098-X
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